{"id":7908,"date":"2026-09-14T21:37:17","date_gmt":"2026-09-14T20:37:17","guid":{"rendered":"https:\/\/www.onlinelearningsystem.net\/xyz\/revision-notes\/a-level-chemistry\/ocr-a\/2-1-1-atomic-structure-and-isotopes\/mass-spectrometry\/identifying-compounds-from-mass-spectra\/"},"modified":"2026-09-22T16:34:04","modified_gmt":"2026-09-22T15:34:04","slug":"identifying-compounds-from-mass-spectra","status":"publish","type":"page","link":"https:\/\/www.onlinelearningsystem.net\/xyz\/revision-notes\/a-level-chemistry\/ocr-a\/2-1-1-atomic-structure-and-isotopes\/mass-spectrometry\/identifying-compounds-from-mass-spectra\/","title":{"rendered":"Identifying Compounds from Mass Spectra"},"content":{"rendered":"\n<section class=\"ols-revision-page ols-identifying-compounds-mass-spectra-page\">\n  <style>\n    .ols-revision-page {\n      --navy: #1C244B;\n      --blue: #2563eb;\n      --soft-blue: #eef4ff;\n      --soft-red: #fff7f7;\n      --soft-purple: #f7f0ff;\n      --soft-green: #f0f7f1;\n 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background: #ffffff; border: 1px solid rgba(28, 36, 75, 0.12); border-radius: 22px; padding: 14px; margin: 18px 0 6px; }\n    .ols-figure-placeholder .ols-figure-caption p { margin: 10px 0 0; font-size: 14px; color: #667085; text-align: center; }\n<\/style>\n\n  <aside class=\"ols-sidebar\">\n  <div class=\"ols-sidebar-header\">\n    <h3>Revision Notes<\/h3>\n    <p>OCR A Level Chemistry A<\/p>\n  <\/div>\n  <div class=\"ols-topic-group\">\n    <h4>2.1.1 Atomic Structure and Isotopes<\/h4>\n    <ul class=\"ols-topic-list\">\n      <li><a href=\"https:\/\/www.onlinelearningsystem.net\/xyz\/revision-notes\/a-level-chemistry\/ocr-a\/2-1-1-atomic-structure-and-isotopes\/\">Section overview<\/a><\/li>\n      <li><a href=\"https:\/\/www.onlinelearningsystem.net\/xyz\/revision-notes\/a-level-chemistry\/ocr-a\/2-1-1-atomic-structure-and-isotopes\/atomic-structure\/\">Atomic Structure<\/a><\/li>\n      <li>\n        <a href=\"https:\/\/www.onlinelearningsystem.net\/xyz\/revision-notes\/a-level-chemistry\/ocr-a\/2-1-1-atomic-structure-and-isotopes\/mass-spectrometry\/\">Mass Spectrometry<\/a>\n        <ul class=\"ols-subtopic-list\">\n          <li><a href=\"https:\/\/www.onlinelearningsystem.net\/xyz\/revision-notes\/a-level-chemistry\/ocr-a\/2-1-1-atomic-structure-and-isotopes\/mass-spectrometry\/the-mass-spectrometer\/\">The Mass Spectrometer<\/a><\/li>\n          <li><a href=\"https:\/\/www.onlinelearningsystem.net\/xyz\/revision-notes\/a-level-chemistry\/ocr-a\/2-1-1-atomic-structure-and-isotopes\/mass-spectrometry\/ram-calculations\/\">RAM Calculations<\/a><\/li>\n          <li><a href=\"https:\/\/www.onlinelearningsystem.net\/xyz\/revision-notes\/a-level-chemistry\/ocr-a\/2-1-1-atomic-structure-and-isotopes\/mass-spectrometry\/predicting-diatomic-mass-spectra\/\">Predicting Diatomic Mass Spectra<\/a><\/li>\n          <li><a href=\"https:\/\/www.onlinelearningsystem.net\/xyz\/revision-notes\/a-level-chemistry\/ocr-a\/2-1-1-atomic-structure-and-isotopes\/mass-spectrometry\/identifying-compounds-from-mass-spectra\/\">Identifying Compounds from Mass Spectra<\/a><\/li>\n        <\/ul>\n      <\/li>\n    <\/ul>\n  <\/div>\n  <div class=\"ols-topic-group\">\n    <h4>Other OCR Sections<\/h4>\n    <ul class=\"ols-topic-list\">\n      <li><a href=\"https:\/\/www.onlinelearningsystem.net\/xyz\/revision-notes\/a-level-chemistry\/ocr-a\/2-2-1-electron-structure\/\">2.2.1 Electron Structure<\/a><\/li>\n      <li><a href=\"https:\/\/www.onlinelearningsystem.net\/xyz\/revision-notes\/a-level-chemistry\/ocr-a\/2-2-2-bonding-and-structure\/\">2.2.2 Bonding and Structure<\/a><\/li>\n      <li><a href=\"https:\/\/www.onlinelearningsystem.net\/xyz\/revision-notes\/a-level-chemistry\/ocr-a\/3-1-1-periodicity\/\">3.1.1 Periodicity<\/a><\/li>\n      <li><a href=\"https:\/\/www.onlinelearningsystem.net\/xyz\/revision-notes\/a-level-chemistry\/ocr-a\/4-1-1-basic-concepts-of-organic-chemistry\/\">4.1.1 Basic Concepts of Organic Chemistry<\/a><\/li>\n      <li><a href=\"https:\/\/www.onlinelearningsystem.net\/xyz\/revision-notes\/a-level-chemistry\/ocr-a\/4-1-2-alkanes\/\">4.1.2 Alkanes<\/a><\/li>\n      <li><a href=\"https:\/\/www.onlinelearningsystem.net\/xyz\/revision-notes\/a-level-chemistry\/ocr-a\/4-1-3-alkenes\/\">4.1.3 Alkenes<\/a><\/li>\n    <\/ul>\n  <\/div>\n<\/aside>\n<script>\r\n(function() {\r\n  function normalisePath(path) {\r\n    return String(path || '')\r\n      .split('?')[0]\r\n      .split('#')[0]\r\n      .replace(\/\\\/+$\/, '')\r\n      .toLowerCase();\r\n  }\r\n\r\n  function highlightActive() {\r\n    var sidebar = document.querySelector('.ols-sidebar');\r\n    if (!sidebar) return false;\r\n\r\n    var currentPath = normalisePath(window.location.pathname);\r\n    var links = 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\/\n<a href=\"https:\/\/www.onlinelearningsystem.net\/xyz\/revision-notes\/a-level-chemistry\/ocr-a\/2-1-1-atomic-structure-and-isotopes\/\">2.1.1 Atomic Structure and Isotopes<\/a> \/\n<a href=\"https:\/\/www.onlinelearningsystem.net\/xyz\/revision-notes\/a-level-chemistry\/ocr-a\/2-1-1-atomic-structure-and-isotopes\/mass-spectrometry\/\">Mass Spectrometry<\/a> \/\n<span>Identifying Compounds from Mass Spectra<\/span>\n<\/nav>\n\n      <header class=\"ols-title-card\">\n        <h1>Identifying Compounds from Mass Spectra<\/h1>\n        <p class=\"ols-page-intro\">A concise revision guide to using the molecular ion peak and peak pattern in a mass spectrum to help identify an unknown compound.<\/p>\n\n        <div class=\"ols-badges\">\n          <div class=\"ols-badge\">Paper 1 and 2<\/div>\n<div class=\"ols-badge\">2.1.1 Atomic Structure and Isotopes<\/div>\n<div class=\"ols-badge\">H432\/01 and H432\/02<\/div>\n        <\/div>\n\n        <div class=\"ols-author\">\n\n    <img decoding=\"async\"\n      class=\"ols-author-avatar-img\"\n      src=\"https:\/\/www.onlinelearningsystem.net\/xyz\/wp-content\/uploads\/2026\/05\/Author-Profile.jpeg\"\n      alt=\"Dr. Mohammed Al-Fatah\"\n    >\n\n    <div class=\"ols-author-content\">\n\n      <h2 class=\"ols-author-title\">\n        Written by: Dr. Mohammed Al-Fatah\n      <\/h2>\n\n      <p class=\"ols-author-description\">\n        Chemistry specialist revision notes for A Level Chemistry.\n      <\/p>\n\n      <a class=\"ols-linkedin-pill\" href=\"https:\/\/www.linkedin.com\/in\/doctormohammedfatah\/\" target=\"_blank\" rel=\"noopener noreferrer\">\n\n        <svg class=\"ols-linkedin-icon\" viewBox=\"0 0 24 24\" fill=\"currentColor\" aria-hidden=\"true\">\n          <path d=\"M4.98 3.5C4.98 4.88 3.86 6 2.48 6S0 4.88 0 3.5 1.12 1 2.48 1s2.5 1.12 2.5 2.5zM.5 8h4V24h-4V8zm7 0h3.8v2.2h.1c.5-.9 1.8-2.2 3.9-2.2 4.2 0 5 2.8 5 6.4V24h-4v-7.6c0-1.8 0-4.2-2.6-4.2s-3 2-3 4v7.8h-4V8z\"\/>\n        <\/svg>\n\n        View LinkedIn Profile\n\n      <\/a>\n\n    <\/div>\n\n  <\/div>\n      <\/header>\n\n      <section class=\"ols-h5p-card ols-h5p-inline ols-h5p-recap\">\n<span class=\"ols-h5p-kicker\">Before you start<\/span>\n<h2>GCSE Recap: Relative Formula Mass<\/h2>\n<p>Before you start, check that you can still calculate a relative formula mass from a formula.<\/p>\n<div class=\"ols-h5p-frame\"><div class=\"h5p-content\" data-content-id=\"605\"><\/div><\/div>\n<\/section>\n<article class=\"ols-note-card soft\">\n<div class=\"ols-note-title\">\n<div class=\"ols-note-icon\">1<\/div>\n<h2>Where This Sits in the OCR Specification<\/h2>\n<\/div>\n<p>OCR examines the molecular ion peak and relative molecular mass of organic compounds in 4.2.4 Analytical techniques (mass spectrometry), not in 2.1.1. Keep this page for that section, where OCR also asks you to use fragmentation peaks to identify parts of a structure.<\/p>\n<\/article>\n<article class=\"ols-note-card soft\">\n        <div class=\"ols-note-title\"><div class=\"ols-note-icon\">2<\/div><h2>What Does Identifying a Compound Mean?<\/h2><\/div>\n        <p>Mass spectrometry can be used to help <strong>identify unknown compounds<\/strong> by analysing the pattern of peaks in their spectra.<\/p>\n        <p>The most important starting point is often the <strong>molecular ion peak<\/strong>, also called the <strong>M<sup>+<\/sup> peak<\/strong>. This peak is caused by the molecular ion formed when one electron is removed from the molecule.<\/p>\n        <div class=\"ols-definition-box\">\n          <p><strong>Molecular ion:<\/strong> the positive ion formed when a molecule loses one electron, usually written as M<sup>+<\/sup>.<\/p>\n        <\/div>\n        <div class=\"ols-key-box\"><p><strong>Key idea:<\/strong> for a 1+ ion, the m\/z value of the molecular ion peak is equal to the relative molecular mass of the compound.<\/p><\/div>\n      <\/article>\n\n      <article class=\"ols-note-card\">\n        <div class=\"ols-note-title\"><div class=\"ols-note-icon\">3<\/div><h2>Use the Molecular Ion Peak to Find Molecular Mass<\/h2><\/div>\n        <p>When a sample is bombarded with electrons in the mass spectrometer, some molecules lose an electron and form molecular ions.<\/p>\n\n        <div class=\"ols-formula-box\">\n          <p>M(g) + e<sup>&#8211;<\/sup> &rarr; M<sup>+<\/sup>(g) + 2e<sup>&#8211;<\/sup><\/p>\n          <small>The molecular ion normally has a single positive charge, so m\/z matches the molecular mass.<\/small>\n        <\/div>\n\n        <p>In a mass spectrum, the molecular ion peak is usually the peak with the <strong>highest significant m\/z value<\/strong>. Small M+1 peaks may appear just above it because of naturally occurring isotopes such as carbon-13, so these are usually ignored when finding the main molecular mass.<\/p>\n\n        <div class=\"ols-key-box\"><p><strong>Exam focus:<\/strong> use the highest significant molecular ion peak, not a small M+1 isotope peak, when identifying the molecular mass.<\/p><\/div>\n      <\/article>\n<section class=\"ols-h5p-card ols-h5p-inline\">\n<span class=\"ols-h5p-kicker\">Check your understanding<\/span>\n<h2>Quick Check: Choosing the Molecular Ion Peak<\/h2>\n<p>Decide which peak gives the molecular mass of a new hydrocarbon and explain the small peak above it.<\/p>\n<div class=\"ols-h5p-frame\"><div class=\"h5p-iframe-wrapper\"><iframe id=\"h5p-iframe-256\" class=\"h5p-iframe\" data-content-id=\"256\" style=\"height:1px\" src=\"about:blank\" frameBorder=\"0\" scrolling=\"no\" title=\"Molecular Ion Peak MCQ: Finding the Molecular Mass When an M+1 Peak Is Present\"><\/iframe><\/div><\/div>\n<\/section>\n\n      <article class=\"ols-note-card purple\">\n        <div class=\"ols-note-title\"><div class=\"ols-note-icon\">4<\/div><h2>Read the Axes Before Interpreting the Spectrum<\/h2><\/div>\n        <p>The <strong>x-axis<\/strong> in a mass spectrum shows the mass-to-charge ratio, written as <strong>m\/z<\/strong>. The <strong>y-axis<\/strong> shows the relative abundance of ions, often expressed as a percentage. The tallest peak is called the <strong>base peak<\/strong>. It comes from the most abundant ion and is given a relative abundance of 100%.<\/p>\n        <p>For most introductory A Level examples, the ions are assumed to have a <strong>1+ charge<\/strong>. This means the m\/z value can be interpreted directly as the mass of that ion.<\/p>\n\n        <div class=\"ols-table-wrap\">\n          <table class=\"ols-table\">\n            <thead>\n              <tr>\n                <th>Feature<\/th>\n                <th>Meaning<\/th>\n                <th>How it helps identify a compound<\/th>\n              <\/tr>\n            <\/thead>\n            <tbody>\n              <tr>\n                <td data-label=\"Feature\">m\/z value<\/td>\n                <td data-label=\"Meaning\">Mass-to-charge ratio of an ion<\/td>\n                <td data-label=\"How it helps identify a compound\">For 1+ ions, it gives the mass of the ion.<\/td>\n              <\/tr>\n              <tr>\n                <td data-label=\"Feature\">Relative abundance<\/td>\n                <td data-label=\"Meaning\">How common each ion is compared with the others<\/td>\n                <td data-label=\"How it helps identify a compound\">The peak pattern can support a suggested structure.<\/td>\n              <\/tr>\n              <tr>\n                <td data-label=\"Feature\">M<sup>+<\/sup> peak<\/td>\n                <td data-label=\"Meaning\">Peak caused by the molecular ion<\/td>\n                <td data-label=\"How it helps identify a compound\">Its m\/z value gives the relative molecular mass.<\/td>\n              <\/tr>\n              <tr>\n                <td data-label=\"Feature\">Base peak<\/td>\n                <td data-label=\"Meaning\">The tallest peak, set at 100% relative abundance<\/td>\n                <td data-label=\"How it helps identify a compound\">It is often a fragment ion, so do not assume it is the M<sup>+<\/sup> peak.<\/td>\n              <\/tr>\n            <\/tbody>\n          <\/table>\n        <\/div>\n      <\/article>\n<section class=\"ols-h5p-card ols-h5p-inline\">\n<span class=\"ols-h5p-kicker\">Check your understanding<\/span>\n<h2>Quick Check: Reading the Axes<\/h2>\n<p>Read the listed peaks of a new spectrum and type a number in each gap.<\/p>\n<div class=\"ols-h5p-frame\"><div class=\"h5p-iframe-wrapper\"><iframe id=\"h5p-iframe-255\" class=\"h5p-iframe\" data-content-id=\"255\" style=\"height:1px\" src=\"about:blank\" frameBorder=\"0\" scrolling=\"no\" title=\"Mass Spectrum Axes Fill in the Blanks: Reading m\/z and Relative Abundance\"><\/iframe><\/div><\/div>\n<\/section>\n\n      <article class=\"ols-note-card orange\">\n        <div class=\"ols-note-title\"><div class=\"ols-note-icon\">5<\/div><h2>Worked Example: Identifying Ethanol<\/h2><\/div>\n        <p>The mass spectrum of an unknown alcohol shows a molecular ion peak at <strong>m\/z 46<\/strong>. Assuming the molecular ion has a 1+ charge, this means the relative molecular mass of the compound is <strong>46<\/strong>.<\/p>\n\n        <div class=\"ols-worked-grid\">\n          <div class=\"ols-worked-step\">\n            <h3>Step 1: Find the molecular ion peak<\/h3>\n            <p>The molecular ion peak is at m\/z 46, so the compound has M<sub>r<\/sub> = 46.<\/p>\n          <\/div>\n          <div class=\"ols-worked-step\">\n            <h3>Step 2: Compare with possible alcohols<\/h3>\n            <p>Ethanol has formula C<sub>2<\/sub>H<sub>5<\/sub>OH, or C<sub>2<\/sub>H<sub>6<\/sub>O.<\/p>\n          <\/div>\n          <div class=\"ols-worked-step\">\n            <h3>Step 3: Calculate the relative molecular mass<\/h3>\n            <p>(2 &times; 12.0) + (6 &times; 1.0) + 16.0 = <strong>46.0<\/strong><\/p>\n          <\/div>\n        <\/div>\n\n        <div class=\"ols-formula-box\">\n          <p>M<sub>r<\/sub> of ethanol = 46.0<\/p>\n          <small>This matches the molecular ion peak at m\/z 46.<\/small>\n        <\/div>\n\n        <div class=\"ols-figure-card\">\n<div class=\"ols-figure-image\"><img decoding=\"async\" src=\"https:\/\/www.onlinelearningsystem.net\/xyz\/wp-content\/uploads\/2026\/09\/fix-16.jpg\" alt=\"Mass spectrum of ethanol with the molecular ion peak at m\/z 46 identified\"><\/div>\n<div class=\"ols-figure-caption\"><p>The molecular ion peak at m\/z 46 matches the relative molecular mass of ethanol, C2H5OH.<\/p><\/div>\n<\/div>\n      <\/article>\n<section class=\"ols-h5p-card ols-h5p-inline\">\n<span class=\"ols-h5p-kicker\">Check your understanding<\/span>\n<h2>Quick Check: Match the Peak to a Formula<\/h2>\n<p>Calculate the relative molecular mass of each candidate on paper before you flip the card.<\/p>\n<div class=\"ols-h5p-frame\"><div class=\"h5p-iframe-wrapper\"><iframe id=\"h5p-iframe-257\" class=\"h5p-iframe\" data-content-id=\"257\" style=\"height:1px\" src=\"about:blank\" frameBorder=\"0\" scrolling=\"no\" title=\"Identifying Compounds Flip Cards: Match the Molecular Ion Peak to a Formula\"><\/iframe><\/div><\/div>\n<\/section>\n\n      <article class=\"ols-note-card\">\n        <div class=\"ols-note-title\"><div class=\"ols-note-icon\">6<\/div><h2>Use the Peak Pattern to Support the Identity<\/h2><\/div>\n        <p>The molecular ion peak gives the molecular mass, but a mass spectrum usually contains other peaks as well. These arise from <strong>fragment ions<\/strong>, produced when the molecular ion breaks apart.<\/p>\n        <p>Fragment peaks can help distinguish compounds with the same molecular mass. For example, different alcohols may produce different fragment ion patterns even if they have the same molecular formula.<\/p>\n        <p>A fragment is assigned from its mass. In the ethanol spectrum, the C-C bond of the molecular ion can break to give CH<sub>2<\/sub>OH<sup>+<\/sup> at <strong>m\/z 31<\/strong> (12 + 2 + 16 + 1) or CH<sub>3<\/sub><sup>+<\/sup> at <strong>m\/z 15<\/strong> (12 + 3). The two pieces add up to the molecular mass: 31 + 15 = 46.<\/p>\n        <div class=\"ols-formula-box\">\n          <p>CH<sub>3<\/sub>CH<sub>2<\/sub>OH<sup>+<\/sup> &rarr; CH<sub>2<\/sub>OH<sup>+<\/sup> + CH<sub>3<\/sub>\u2022<\/p>\n          <small>Only the charged fragment is detected. The CH<sub>3<\/sub>\u2022 radical has no charge, so it gives no peak.<\/small>\n        <\/div>\n        <p>In ethanol the peak at m\/z 31 is the base peak, so here the tallest peak is a fragment and not the molecular ion.<\/p>\n        <div class=\"ols-key-box\"><p><strong>Key idea:<\/strong> molecular ion peak first, then peak pattern. The molecular ion peak gives molecular mass, while fragment peaks help support the identity or structure.<\/p><\/div>\n      <\/article>\n<section class=\"ols-h5p-card ols-h5p-inline\">\n<span class=\"ols-h5p-kicker\">Check your understanding<\/span>\n<h2>Quick Check: Tallest Peak or Molecular Ion Peak?<\/h2>\n<p>Decide what a new spectrum tells you when the tallest peak is not the one with the highest m\/z value.<\/p>\n<div class=\"ols-h5p-frame\"><div class=\"h5p-iframe-wrapper\"><iframe id=\"h5p-iframe-258\" class=\"h5p-iframe\" data-content-id=\"258\" style=\"height:1px\" src=\"about:blank\" frameBorder=\"0\" scrolling=\"no\" title=\"Molecular Ion Peak MCQ: When the Tallest Peak Is a Fragment\"><\/iframe><\/div><\/div>\n<\/section>\n<section class=\"ols-h5p-card ols-h5p-inline\">\n<span class=\"ols-h5p-kicker\">Check your understanding<\/span>\n<h2>Quick Check: How Far Does the Evidence Go?<\/h2>\n<p>In each round, pick the one statement that is accurate.<\/p>\n<div class=\"ols-h5p-frame\"><div class=\"h5p-iframe-wrapper\"><iframe id=\"h5p-iframe-606\" class=\"h5p-iframe\" data-content-id=\"606\" style=\"height:1px\" src=\"about:blank\" frameBorder=\"0\" scrolling=\"no\" title=\"Identifying Compounds Summary: How Far the Evidence from a Mass Spectrum Goes\"><\/iframe><\/div><\/div>\n<\/section>\n\n      <article class=\"ols-note-card purple\">\n        <div class=\"ols-note-title\"><div class=\"ols-note-icon\">7<\/div><h2>Common Exam Points<\/h2><\/div>\n        <p>These points help avoid common mistakes when interpreting mass spectra of unknown compounds.<\/p>\n\n        <div class=\"ols-rule-list\">\n          <div class=\"ols-rule-item\"><h3>Do not confuse the base peak with the molecular ion peak<\/h3><p>The base peak is the tallest peak. The molecular ion peak is the peak caused by the whole molecule after losing one electron. They are not always the same peak.<\/p><\/div>\n          <div class=\"ols-rule-item\"><h3>Use the highest significant m\/z value<\/h3><p>The molecular ion peak is usually at the highest significant m\/z value. Small M+1 peaks can occur due to carbon-13 and should not normally be used as the main molecular mass.<\/p><\/div>\n          <div class=\"ols-rule-item\"><h3>State the charge assumption<\/h3><p>For a 1+ molecular ion, m\/z is equal to the molecular mass. If the charge were different, the relationship would change.<\/p><\/div>\n          <div class=\"ols-rule-item\"><h3>Show the molecular mass calculation<\/h3><p>When suggesting a compound, calculate its M<sub>r<\/sub> and compare it directly with the molecular ion peak.<\/p><\/div>\n        <\/div>\n      <\/article>\n\n      \n\n      <section class=\"ols-quicksnap-card\">\n        <h2>QuickSnap Summary<\/h2>\n        <p>Identifying a compound from a mass spectrum starts with the molecular ion peak, then uses the wider peak pattern to support the proposed identity.<\/p>\n\n        <div class=\"ols-snap-list\">\n          <div class=\"ols-snap-item\"><div class=\"ols-snap-number\">1<\/div><p>Find the molecular ion, M<sup>+<\/sup>, peak in the spectrum.<\/p><\/div>\n          <div class=\"ols-snap-item\"><div class=\"ols-snap-number\">2<\/div><p>For a 1+ ion, use the m\/z value of the molecular ion peak as the molecular mass.<\/p><\/div>\n          <div class=\"ols-snap-item\"><div class=\"ols-snap-number\">3<\/div><p>Compare the molecular mass with possible compounds by calculating their M<sub>r<\/sub> values.<\/p><\/div>\n          <div class=\"ols-snap-item\"><div class=\"ols-snap-number\">4<\/div><p>Use fragment peaks and the overall peak pattern as supporting evidence for the proposed compound.<\/p><\/div>\n        <\/div>\n      <\/section>\n\n      <section class=\"ols-faq-card\">\n        <h2>FAQs<\/h2>\n        <p>These questions focus on the main exam points for identifying compounds from mass spectra.<\/p>\n\n        <div class=\"ols-faq-list\">\n          <div class=\"ols-faq-item\">\n            <h3>What is the molecular ion peak?<\/h3>\n            <p>The molecular ion peak is the peak caused by the whole molecule after it has lost one electron. It is often written as the M<sup>+<\/sup> peak.<\/p>\n          <\/div>\n          <div class=\"ols-faq-item\">\n            <h3>How does the molecular ion peak identify molecular mass?<\/h3>\n            <p>If the molecular ion has a 1+ charge, the m\/z value of the molecular ion peak is equal to the relative molecular mass of the compound.<\/p>\n          <\/div>\n          <div class=\"ols-faq-item\">\n            <h3>Why might there be a small peak after the M<sup>+<\/sup> peak?<\/h3>\n            <p>A small M+1 peak can occur because of naturally occurring heavier isotopes, such as carbon-13. This should not normally be used as the main molecular ion peak.<\/p>\n          <\/div>\n          <div class=\"ols-faq-item\">\n            <h3>Why is ethanol identified from a molecular ion peak at m\/z 46?<\/h3>\n            <p>Ethanol has formula C<sub>2<\/sub>H<sub>5<\/sub>OH. Its relative molecular mass is (2 &times; 12.0) + (6 &times; 1.0) + 16.0 = 46.0, matching the molecular ion peak at m\/z 46.<\/p>\n          <\/div>\n          <div class=\"ols-faq-item\">\n            <h3>Are fragment peaks useful for identification?<\/h3>\n            <p>Yes. Fragment peaks help support the proposed structure because different compounds can break into different characteristic ions.<\/p>\n          <\/div>\n        <\/div>\n      <\/section>\n\n      <section class=\"ols-related-card\">\n        <h2>Related Topics<\/h2>\n        <p>Use these related pages to strengthen your understanding of mass spectrometry and isotope analysis.<\/p>\n\n        <div class=\"ols-related-grid\">\n          <a class=\"ols-related-item\" href=\"https:\/\/www.onlinelearningsystem.net\/xyz\/revision-notes\/a-level-chemistry\/ocr-a\/2-1-1-atomic-structure-and-isotopes\/mass-spectrometry\/the-mass-spectrometer\/\">The Mass Spectrometer<\/a>\n          <a class=\"ols-related-item\" href=\"https:\/\/www.onlinelearningsystem.net\/xyz\/revision-notes\/a-level-chemistry\/ocr-a\/2-1-1-atomic-structure-and-isotopes\/mass-spectrometry\/ram-calculations\/\">RAM Calculations<\/a>\n          <a class=\"ols-related-item\" href=\"https:\/\/www.onlinelearningsystem.net\/xyz\/revision-notes\/a-level-chemistry\/ocr-a\/2-1-1-atomic-structure-and-isotopes\/mass-spectrometry\/predicting-diatomic-mass-spectra\/\">Predicting Diatomic Mass Spectra<\/a>\n        <\/div>\n      <\/section>\n\n      <section class=\"ols-course-cta-atomic\" id=\"olsCourseCtaAtomic001\">\r\n  <style>\r\n    .ols-course-cta-atomic,\r\n    .ols-course-cta-atomic * {\r\n      box-sizing: border-box;\r\n    }\r\n\r\n    .ols-course-cta-atomic {\r\n      --navy: #1C244B;\r\n      --blue: #2563eb;\r\n      --body-text: #1f2937;\r\n      --grey-text: #667085;\r\n      --border: rgba(28, 36, 75, 0.14);\r\n      --shadow: 0 18px 45px rgba(28, 36, 75, 0.12);\r\n      --inner-shadow: 0 10px 26px rgba(28, 36, 75, 0.08);\r\n\r\n      width: 100%;\r\n      margin: 30px 0 24px;\r\n      font-family: Poppins, Arial, sans-serif;\r\n    }\r\n\r\n    .ols-course-cta-atomic .ols-course-cta-card {\r\n      overflow: hidden;\r\n      border-radius: 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href=\"https:\/\/www.onlinelearningsystem.net\/xyz\/product\/atomic-structure-and-the-periodic-table-2-1-1-ocr-a\/\" aria-label=\"Open the OCR A Level Chemistry A 2.1.1, 2.2.1 and 3.1.1 Atomic Structure and the Periodic Table course page\">\r\n\r\n        <div class=\"ols-course-cta-image\">\r\n          <img decoding=\"async\"\r\n            src=\"https:\/\/www.onlinelearningsystem.net\/xyz\/wp-content\/uploads\/2026\/09\/ocr-a-level-chemistry-a-2-1-1-atomic-structure-interactive-course-banner.jpg\"\r\n            alt=\"OCR A Level Chemistry A 2.1.1, 2.2.1 and 3.1.1 Atomic Structure and the Periodic Table interactive course banner\"\r\n          >\r\n        <\/div>\r\n\r\n      <\/a>\r\n\r\n      <div class=\"ols-course-cta-content\">\r\n\r\n        <div class=\"ols-course-cta-header-row\">\r\n\r\n          <div class=\"ols-course-cta-kicker\">\r\n            OCR H432 | 2.1.1, 2.2.1 and 3.1.1 Course\r\n          <\/div>\r\n\r\n          <a class=\"ols-course-button ols-course-button-top\" href=\"https:\/\/www.onlinelearningsystem.net\/xyz\/product\/atomic-structure-and-the-periodic-table-2-1-1-ocr-a\/\">\r\n            View Course\r\n          <\/a>\r\n\r\n        <\/div>\r\n\r\n        <h2>\r\n          Master Atomic Structure and the Periodic Table for OCR A Level Chemistry A\r\n        <\/h2>\r\n\r\n      <\/div>\r\n\r\n    <\/div>\r\n\r\n    <div class=\"ols-course-cta-intro-stats\">\r\n\r\n      <p class=\"ols-course-cta-intro\">\r\n        Continue from these free revision notes into the full 2.1.1, 2.2.1 and 3.1.1 Atomic Structure and the Periodic Table course. The guided video lessons are ready now; the OCR A MCQ bank, teacher-marked short-answer questions and KASP spec-point report are being written, and the course opens for enrolment as soon as they are complete.\r\n      <\/p>\r\n\r\n      <div class=\"ols-course-cta-stats\">\r\n\r\n        <div class=\"ols-course-stat\">\r\n          <span>Recorded lessons<\/span>\n          <strong>Coming soon<\/strong>\r\n        <\/div>\r\n\r\n        <div class=\"ols-course-stat\">\r\n          <span>Video lessons<\/span>\n          <strong>Coming soon<\/strong>\r\n        <\/div>\r\n\r\n        <div class=\"ols-course-stat\">\r\n          <span>MCQ practice<\/span>\n          <strong>Coming soon<\/strong>\r\n        <\/div>\r\n\r\n        <div class=\"ols-course-stat\">\r\n          <span>SAQ practice<\/span>\n          <strong>Coming soon<\/strong>\r\n        <\/div>\r\n\r\n      <\/div>\r\n\r\n    <\/div>\r\n\r\n    <div class=\"ols-course-cta-features\">\r\n\r\n      <div class=\"ols-course-feature\">\r\n        <h3>Guided video teaching<\/h3>\r\n        <p>\r\n          Learn the chemistry and exam technique through structured video lessons with worked examples and walkthroughs.\r\n        <\/p>\r\n      <\/div>\r\n\r\n      <div class=\"ols-course-feature\">\r\n        <h3>Instant MCQ feedback<\/h3>\r\n        <p>\r\n          Auto-marked MCQ quizzes provide immediate diagnostic feedback for every answer choice.\r\n        <\/p>\r\n      <\/div>\r\n\r\n      <div class=\"ols-course-feature\">\r\n        <h3>Teacher-marked SAQs<\/h3>\r\n        <p>\r\n          Submit written exam responses and receive chemistry specialist feedback with improvement guidance.\r\n        <\/p>\r\n      <\/div>\r\n\r\n      <div class=\"ols-course-feature\">\r\n        <h3>Progress tracking<\/h3>\r\n        <p>\r\n          Identify strengths and weaknesses across the full 2.1.1, 2.2.1 and 3.1.1 specification with targeted reporting.\r\n        <\/p>\r\n      <\/div>\r\n\r\n    <\/div>\r\n\r\n    <div class=\"ols-course-animation-wrap\">\r\n\r\n      <h3 class=\"ols-course-animation-title\">\r\n        See how the course works\r\n      <\/h3>\r\n\r\n      <div class=\"ols-animation-frame-shell\">\r\n        <iframe\r\n          id=\"olsCourseAnimationFrame001\"\r\n          title=\"OLS course preview animation\"\r\n          loading=\"lazy\"\r\n          referrerpolicy=\"no-referrer\">\r\n        <\/iframe>\r\n\r\n        <button\r\n          class=\"ols-animation-start-overlay\"\r\n          id=\"olsCourseAnimationStart001\"\r\n          type=\"button\"\r\n          aria-label=\"Play OLS course preview animation\">\r\n          <span class=\"ols-animation-start-content\">\r\n            <span class=\"ols-animation-play-circle\" aria-hidden=\"true\">\r\n              <span class=\"ols-animation-play-icon\"><\/span>\r\n            <\/span>\r\n            <span class=\"ols-animation-start-text\">\r\n              Play course preview animation\r\n            <\/span>\r\n          <\/span>\r\n        <\/button>\r\n\r\n        <button\r\n          class=\"ols-animation-pause-button\"\r\n          id=\"olsCourseAnimationPause001\"\r\n          type=\"button\"\r\n          aria-label=\"Pause course preview animation\">\r\n          Pause\r\n        <\/button>\r\n      <\/div>\r\n\r\n      <p class=\"ols-course-video-status\">\r\n        Click play to start the course preview animation.\r\n      <\/p>\r\n\r\n    <\/div>\r\n\r\n    <div class=\"ols-course-cta-bottom\">\r\n\r\n      <a class=\"ols-course-button\" href=\"https:\/\/www.onlinelearningsystem.net\/xyz\/product\/atomic-structure-and-the-periodic-table-2-1-1-ocr-a\/\">\r\n        View Atomic Structure and the Periodic Table Course\r\n      <\/a>\r\n\r\n    <\/div>\r\n\r\n  <\/div>\r\n\r\n  <template id=\"olsCourseAnimationTemplate001\">\r\n<!DOCTYPE html>\r\n<html lang=\"en\">\r\n<head>\r\n<meta charset=\"UTF-8\">\r\n<meta name=\"viewport\" content=\"width=device-width, initial-scale=1.0\">\r\n<title>OLS Combined Promo Animation<\/title>\r\n\r\n<style>\r\n*{box-sizing:border-box;}\r\n\r\nhtml.ols-animation-paused *,\r\nhtml.ols-animation-paused *::before,\r\nhtml.ols-animation-paused *::after{\r\n  animation-play-state:paused!important;\r\n}\r\n\r\n:root{\r\n  --ols-video-screen-w:1180;\r\n  --ols-video-screen-h:664;\r\n  --ols-video-screen-scale:1;\r\n  --ols-mcq-screen-w:1360;\r\n  --ols-mcq-screen-h:1130;\r\n  --ols-mcq-screen-scale:1;\r\n  --ols-saq-screen-w:1360;\r\n  --ols-saq-screen-h:965;\r\n  --ols-saq-screen-scale:1;\r\n}\r\n\r\nhtml,\r\nbody{\r\n  width:100%;\r\n  height:100%;\r\n}\r\n\r\nbody{\r\n  margin:0;\r\n  overflow:hidden;\r\n  font-family:Poppins,Arial,sans-serif;\r\n  background:#e9efff;\r\n}\r\n\r\n.ols-combined-stage{\r\n  position:relative;\r\n  width:100vw;\r\n  height:100vh;\r\n  overflow:hidden;\r\n  background:\r\n    radial-gradient(circle at top left,rgba(70,127,247,0.14),transparent 34%),\r\n    linear-gradient(135deg,#f8fbff 0%,#e9efff 100%);\r\n}\r\n\r\n.ols-scene{\r\n  position:absolute;\r\n  inset:0;\r\n  width:100vw;\r\n  height:100vh;\r\n  opacity:0;\r\n  visibility:hidden;\r\n  pointer-events:none;\r\n}\r\n\r\n.ols-scene.active{\r\n  opacity:1;\r\n  visibility:visible;\r\n  pointer-events:auto;\r\n}\r\n\r\n.ols-scene.fade-out{\r\n  animation:olsSceneFadeOut 0.85s ease forwards;\r\n}\r\n\r\n@keyframes olsSceneFadeOut{\r\n  to{\r\n    opacity:0;\r\n    visibility:hidden;\r\n  }\r\n}\r\n\r\n.ols-title-cursor{\r\n  display:inline-block;\r\n  width:5px;\r\n  height:0.85em;\r\n  background:#1C244B;\r\n  margin-left:8px;\r\n  transform:translateY(8px);\r\n  animation:olsBlink 0.8s infinite;\r\n}\r\n\r\n.cursor{\r\n  display:inline-block;\r\n  width:3px;\r\n  height:28px;\r\n  background:#1c244b;\r\n  margin-left:3px;\r\n  transform:translateY(5px);\r\n  animation:olsBlink 0.8s infinite;\r\n}\r\n\r\n@keyframes olsBlink{\r\n  0%,45%{opacity:1;}\r\n  46%,100%{opacity:0;}\r\n}\r\n\r\n.ols-video-stage,\r\n.ols-mcq-stage,\r\n.ols-saq-stage{\r\n  width:100vw;\r\n  height:100vh;\r\n  display:flex;\r\n  justify-content:center;\r\n  align-items:center;\r\n  padding:0;\r\n  overflow:hidden;\r\n  background:\r\n    radial-gradient(circle at top left,rgba(70,127,247,0.14),transparent 34%),\r\n    linear-gradient(135deg,#f8fbff 0%,#e9efff 100%);\r\n}\r\n\r\n.ols-video-title-screen,\r\n.ols-mcq-intro-screen,\r\n.ols-saq-intro{\r\n  position:absolute;\r\n  inset:0;\r\n  z-index:50;\r\n  display:flex;\r\n  justify-content:center;\r\n  align-items:center;\r\n  background:\r\n    radial-gradient(circle at top left,rgba(70,127,247,0.14),transparent 34%),\r\n    linear-gradient(135deg,#f8fbff 0%,#e9efff 100%);\r\n  opacity:1;\r\n  visibility:visible;\r\n  pointer-events:none;\r\n}\r\n\r\n.ols-video-title-screen.hide{animation:olsVideoTitleFadeOut 0.85s ease forwards;}\r\n.ols-mcq-intro-screen.hide{animation:olsMcqIntroFadeOut 0.85s ease forwards;}\r\n.ols-saq-intro.hide{animation:olsSaqIntroFadeOut 0.85s ease forwards;}\r\n\r\n@keyframes olsVideoTitleFadeOut{to{opacity:0;visibility:hidden;}}\r\n@keyframes olsMcqIntroFadeOut{to{opacity:0;visibility:hidden;}}\r\n@keyframes olsSaqIntroFadeOut{to{opacity:0;visibility:hidden;}}\r\n\r\n.ols-video-title-wrap,\r\n.ols-mcq-intro-title-wrap,\r\n.ols-saq-intro-title-wrap{\r\n  max-width:1250px;\r\n  padding:0 34px;\r\n  text-align:center;\r\n}\r\n\r\n.ols-video-title,\r\n.ols-mcq-intro-title,\r\n.ols-saq-intro-title{\r\n  margin:0;\r\n  font-family:Poppins,Arial,sans-serif;\r\n  font-size:clamp(52px,8vw,124px);\r\n  font-weight:600;\r\n  line-height:1.08;\r\n  color:#1C244B;\r\n  text-shadow:-9px 0 9px rgba(28,36,75,0.16);\r\n  letter-spacing:-0.045em;\r\n}\r\n\r\n#videoTitleText,\r\n#mcqIntroTitleText,\r\n#saqIntroTitleText{\r\n  white-space:pre-wrap;\r\n}\r\n\r\n.ols-video-scene{\r\n  width:100%;\r\n  height:100%;\r\n  display:flex;\r\n  justify-content:center;\r\n  align-items:center;\r\n  opacity:0;\r\n  visibility:hidden;\r\n}\r\n\r\n.ols-video-scene.show{\r\n  visibility:visible;\r\n  animation:olsVideoSceneIn 1s ease forwards;\r\n}\r\n\r\n@keyframes olsVideoSceneIn{to{opacity:1;}}\r\n\r\n.ols-video-scale-wrap{\r\n  width:calc(var(--ols-video-screen-w) * 1px);\r\n  height:calc(var(--ols-video-screen-h) * 1px);\r\n  transform:scale(var(--ols-video-screen-scale));\r\n  transform-origin:center center;\r\n  display:flex;\r\n  justify-content:center;\r\n  align-items:center;\r\n}\r\n\r\n.ols-video-card{\r\n  width:1180px;\r\n  height:664px;\r\n  border-radius:28px;\r\n  overflow:hidden;\r\n  background:#1C244B;\r\n  box-shadow:0 28px 80px rgba(28,36,75,0.28);\r\n  transform:translateY(24px) scale(0.96);\r\n  opacity:0;\r\n}\r\n\r\n.ols-video-scene.show .ols-video-card{\r\n  animation:olsVideoCardIn 1s cubic-bezier(.18,.89,.32,1.12) forwards;\r\n  animation-delay:0.2s;\r\n}\r\n\r\n@keyframes olsVideoCardIn{\r\n  to{\r\n    transform:translateY(0) scale(1);\r\n    opacity:1;\r\n  }\r\n}\r\n\r\n.ols-video-card video{\r\n  display:block;\r\n  width:100%;\r\n  height:100%;\r\n  aspect-ratio:16 \/ 9;\r\n  object-fit:cover;\r\n  border:0;\r\n}\r\n\r\n.ols-mcq-scale-wrap,\r\n.ols-saq-scale-wrap{\r\n  width:calc(var(--ols-mcq-screen-w) * 1px);\r\n  height:calc(var(--ols-mcq-screen-h) * 1px);\r\n  transform:scale(var(--ols-mcq-screen-scale));\r\n  transform-origin:center center;\r\n  display:flex;\r\n  justify-content:center;\r\n  align-items:flex-start;\r\n}\r\n\r\n.ols-saq-scale-wrap{\r\n  width:calc(var(--ols-saq-screen-w) * 1px);\r\n  height:calc(var(--ols-saq-screen-h) * 1px);\r\n  transform:scale(var(--ols-saq-screen-scale));\r\n}\r\n\r\n.ols-mcq-screen{\r\n  width:1360px;\r\n  height:1130px;\r\n  border-radius:22px;\r\n  overflow:hidden;\r\n  background:#eaf0ff;\r\n  box-shadow:0 26px 70px rgba(28,36,75,0.22);\r\n  opacity:0;\r\n  transform:translateY(24px) scale(0.96);\r\n}\r\n\r\n.ols-mcq-screen.show{\r\n  animation:olsMcqScreenEnter 1s ease forwards;\r\n}\r\n\r\n@keyframes olsMcqScreenEnter{\r\n  from{opacity:0;transform:translateY(24px) scale(0.96);}\r\n  to{opacity:1;transform:translateY(0) scale(1);}\r\n}\r\n\r\n.mcq-question-area{\r\n  background:#eaf0ff;\r\n  padding:28px 30px 30px;\r\n  position:relative;\r\n  height:610px;\r\n}\r\n\r\n.mcq-question-lead{\r\n  margin:0 0 14px;\r\n  font-size:24px;\r\n  line-height:1.35;\r\n  color:#111827;\r\n}\r\n\r\n.mcq-ionic-table{\r\n  border-collapse:collapse;\r\n  width:500px;\r\n  margin-bottom:8px;\r\n  font-size:21px;\r\n  color:#111827;\r\n}\r\n\r\n.mcq-ionic-table th,\r\n.mcq-ionic-table td{\r\n  border:1.5px solid #c9ced8;\r\n  padding:12px 18px;\r\n  text-align:center;\r\n}\r\n\r\n.mcq-ionic-table th{\r\n  background:#f2f2f2;\r\n  font-weight:700;\r\n}\r\n\r\n.mcq-ionic-table td{\r\n  background:#eaf0ff;\r\n}\r\n\r\n.mcq-question-main{\r\n  margin:6px 0 28px;\r\n  font-size:24px;\r\n  line-height:1.35;\r\n  color:#111827;\r\n}\r\n\r\n.mcq-options-wrap{\r\n  display:flex;\r\n  flex-direction:column;\r\n  gap:17px;\r\n  max-width:1200px;\r\n}\r\n\r\n.mcq-option-row{\r\n  display:flex;\r\n  align-items:center;\r\n  min-height:34px;\r\n  position:relative;\r\n}\r\n\r\n.mcq-radio{\r\n  width:28px;\r\n  height:28px;\r\n  border-radius:50%;\r\n  border:2px solid #6b7280;\r\n  margin-right:16px;\r\n  background:transparent;\r\n  position:relative;\r\n  flex:0 0 auto;\r\n}\r\n\r\n.mcq-radio::after{\r\n  content:\"\";\r\n  position:absolute;\r\n  inset:5px;\r\n  border-radius:50%;\r\n  background:#6b7280;\r\n  opacity:0;\r\n  transform:scale(0.4);\r\n  transition:opacity 0.25s ease,transform 0.25s ease;\r\n}\r\n\r\n.mcq-option-row.selected .mcq-radio::after{\r\n  opacity:1;\r\n  transform:scale(1);\r\n}\r\n\r\n.mcq-radio-ripple{\r\n  position:absolute;\r\n  left:14px;\r\n  top:50%;\r\n  width:28px;\r\n  height:28px;\r\n  border-radius:50%;\r\n  border:2px solid rgba(28,36,75,0.28);\r\n  transform:translate(-50%,-50%) scale(1);\r\n  opacity:0;\r\n  pointer-events:none;\r\n}\r\n\r\n.mcq-option-row.clicking .mcq-radio-ripple{\r\n  animation:mcqRipple 0.75s ease forwards;\r\n}\r\n\r\n@keyframes mcqRipple{\r\n  0%{opacity:0.65;transform:translate(-50%,-50%) scale(1);}\r\n  100%{opacity:0;transform:translate(-50%,-50%) scale(2.5);}\r\n}\r\n\r\n.mcq-option-label{\r\n  font-size:23px;\r\n  color:#111827;\r\n}\r\n\r\n.mcq-specific-feedback{\r\n  display:inline-flex;\r\n  align-items:center;\r\n  margin-left:18px;\r\n  min-height:38px;\r\n  opacity:0;\r\n  transform:translateX(-8px);\r\n}\r\n\r\n.mcq-specific-feedback.show{\r\n  opacity:1;\r\n  transform:translateX(0);\r\n  transition:opacity 0.35s ease,transform 0.35s ease;\r\n}\r\n\r\n.mcq-cross-icon{\r\n  width:26px;\r\n  height:26px;\r\n  border-radius:50%;\r\n  border:2px solid #d83255;\r\n  color:#d83255;\r\n  display:inline-flex;\r\n  justify-content:center;\r\n  align-items:center;\r\n  font-size:18px;\r\n  font-weight:700;\r\n  margin-right:12px;\r\n  opacity:0;\r\n  transform:scale(0.4);\r\n}\r\n\r\n.mcq-cross-icon.show{\r\n  animation:mcqCrossPop 0.35s ease forwards;\r\n}\r\n\r\n@keyframes mcqCrossPop{\r\n  70%{opacity:1;transform:scale(1.18);}\r\n  100%{opacity:1;transform:scale(1);}\r\n}\r\n\r\n.mcq-specific-feedback-text{\r\n  display:inline-block;\r\n  background:#fff4b8;\r\n  color:#111827;\r\n  padding:8px 16px;\r\n  font-size:22px;\r\n  line-height:1.35;\r\n  min-width:850px;\r\n  min-height:44px;\r\n}\r\n\r\n.mcq-submit-button{\r\n  position:absolute;\r\n  right:34px;\r\n  bottom:30px;\r\n  border:0;\r\n  border-radius:999px;\r\n  background:#1C244B;\r\n  color:#ffffff;\r\n  padding:14px 28px;\r\n  font-size:18px;\r\n  font-weight:600;\r\n  box-shadow:0 14px 32px rgba(28,36,75,0.25);\r\n  cursor:default;\r\n  transition:transform 0.2s ease,box-shadow 0.2s ease,background 0.2s ease;\r\n}\r\n\r\n.mcq-submit-button.clicked{\r\n  transform:translateY(2px) scale(0.97);\r\n  background:#26315f;\r\n  box-shadow:0 7px 18px rgba(28,36,75,0.22);\r\n}\r\n\r\n.mcq-general-feedback{\r\n  height:520px;\r\n  background:#fff3c9;\r\n  color:#8a6a00;\r\n  padding:26px 30px 28px;\r\n  font-size:23px;\r\n  line-height:1.34;\r\n  opacity:0;\r\n  transform:translateY(20px);\r\n  transition:opacity 0.7s ease,transform 0.7s ease;\r\n  overflow:hidden;\r\n}\r\n\r\n.mcq-general-feedback.show{\r\n  opacity:1;\r\n  transform:translateY(0);\r\n}\r\n\r\n#mcqGeneralText{\r\n  white-space:pre-wrap;\r\n}\r\n\r\n.mcq-specific-cursor{background:#111827;}\r\n.mcq-general-cursor{background:#8a6a00;}\r\n\r\n.ols-saq-screen{\r\n  width:1360px;\r\n  height:965px;\r\n  border-radius:22px;\r\n  overflow:hidden;\r\n  background:#eaf0ff;\r\n  box-shadow:0 26px 70px rgba(28,36,75,0.22);\r\n  opacity:0;\r\n  transform:translateY(24px) scale(0.96);\r\n}\r\n\r\n.ols-saq-screen.show{\r\n  animation:olsSaqScreenEnter 1s ease forwards;\r\n}\r\n\r\n@keyframes olsSaqScreenEnter{\r\n  from{opacity:0;transform:translateY(24px) scale(0.96);}\r\n  to{opacity:1;transform:translateY(0) scale(1);}\r\n}\r\n\r\n.saq-question-area{\r\n  height:335px;\r\n  background:#eaf0ff;\r\n  padding:30px 40px 32px;\r\n}\r\n\r\n.saq-question-text{\r\n  font-size:25px;\r\n  line-height:1.42;\r\n  color:#111827;\r\n  margin-bottom:22px;\r\n}\r\n\r\n.saq-student-box{\r\n  height:195px;\r\n  background:#f3f4f6;\r\n  border:2px solid #cfd6e3;\r\n  border-radius:8px;\r\n  padding:23px 26px;\r\n  font-size:24px;\r\n  line-height:1.55;\r\n  color:#4b5563;\r\n  position:relative;\r\n  overflow:hidden;\r\n}\r\n\r\n.saq-teacher-feedback{\r\n  height:630px;\r\n  background:#dff3e6;\r\n  color:#075f3b;\r\n  padding:28px 40px 30px;\r\n  font-size:23px;\r\n  line-height:1.47;\r\n  opacity:0;\r\n  transform:translateY(20px);\r\n  transition:opacity 0.7s ease,transform 0.7s ease;\r\n  overflow:hidden;\r\n}\r\n\r\n.saq-teacher-feedback.show{\r\n  opacity:1;\r\n  transform:translateY(0);\r\n}\r\n\r\n#saqTeacherText{\r\n  white-space:pre-wrap;\r\n}\r\n\r\n.saq-teacher-cursor{\r\n  background:#075f3b;\r\n}\r\n\r\n@media(max-width:900px){\r\n  .ols-video-title,\r\n  .ols-mcq-intro-title,\r\n  .ols-saq-intro-title{\r\n    font-size:clamp(42px,11vw,78px);\r\n    line-height:1.12;\r\n  }\r\n\r\n  .ols-title-cursor{\r\n    width:4px;\r\n    margin-left:6px;\r\n  }\r\n\r\n  .ols-video-card{\r\n    border-radius:20px;\r\n  }\r\n}\r\n<\/style>\r\n<\/head>\r\n\r\n<body>\r\n<div class=\"ols-combined-stage\">\r\n\r\n  <section id=\"sceneVideo\" class=\"ols-scene active\">\r\n    <div class=\"ols-video-stage\">\r\n      <div id=\"videoTitleScreen\" class=\"ols-video-title-screen\">\r\n        <div class=\"ols-video-title-wrap\">\r\n          <h1 class=\"ols-video-title\">\r\n            <span id=\"videoTitleText\"><\/span><span id=\"videoTitleCursor\" class=\"ols-title-cursor\"><\/span>\r\n          <\/h1>\r\n        <\/div>\r\n      <\/div>\r\n\r\n      <section id=\"videoScene\" class=\"ols-video-scene\">\r\n        <div class=\"ols-video-scale-wrap\">\r\n          <div class=\"ols-video-card\">\r\n            <video\r\n              id=\"lessonVideo\"\r\n              src=\"https:\/\/www.onlinelearningsystem.net\/xyz\/wp-content\/uploads\/2026\/05\/Virtual-Lesson.mp4\"\r\n              muted\r\n              playsinline\r\n              preload=\"auto\">\r\n            <\/video>\r\n          <\/div>\r\n        <\/div>\r\n      <\/section>\r\n    <\/div>\r\n  <\/section>\r\n\r\n  <section id=\"sceneMcq\" class=\"ols-scene\">\r\n    <div class=\"ols-mcq-stage\">\r\n      <div id=\"mcqIntroScreen\" class=\"ols-mcq-intro-screen\">\r\n        <div class=\"ols-mcq-intro-title-wrap\">\r\n          <h1 class=\"ols-mcq-intro-title\">\r\n            <span id=\"mcqIntroTitleText\"><\/span><span id=\"mcqIntroTitleCursor\" class=\"ols-title-cursor\"><\/span>\r\n          <\/h1>\r\n        <\/div>\r\n      <\/div>\r\n\r\n      <div class=\"ols-mcq-scale-wrap\">\r\n        <main id=\"mcqScreen\" class=\"ols-mcq-screen\">\r\n          <section class=\"mcq-question-area\">\r\n            <p class=\"mcq-question-lead\">Some ionic radii are shown.<\/p>\r\n\r\n            <table class=\"mcq-ionic-table\">\r\n              <thead>\r\n                <tr>\r\n                  <th>Ion<\/th>\r\n                  <th>Ionic radius \/ nm<\/th>\r\n                <\/tr>\r\n              <\/thead>\r\n              <tbody>\r\n                <tr><td>Na<sup>+<\/sup><\/td><td>0.102<\/td><\/tr>\r\n                <tr><td>K<sup>+<\/sup><\/td><td>0.138<\/td><\/tr>\r\n                <tr><td>F<sup>\u2212<\/sup><\/td><td>0.133<\/td><\/tr>\r\n                <tr><td>Cl<sup>\u2212<\/sup><\/td><td>0.180<\/td><\/tr>\r\n              <\/tbody>\r\n            <\/table>\r\n\r\n            <p class=\"mcq-question-main\">Which compound has the strongest ionic bonding?<\/p>\r\n\r\n            <div class=\"mcq-options-wrap\">\r\n              <div id=\"mcqWrongOption\" class=\"mcq-option-row\">\r\n                <span class=\"mcq-radio\"><\/span>\r\n                <span class=\"mcq-radio-ripple\"><\/span>\r\n                <span class=\"mcq-option-label\">sodium chloride<\/span>\r\n\r\n                <span id=\"mcqSpecificFeedback\" class=\"mcq-specific-feedback\">\r\n                  <span id=\"mcqCrossIcon\" class=\"mcq-cross-icon\">\u00d7<\/span>\r\n                  <span class=\"mcq-specific-feedback-text\">\r\n                    <span id=\"mcqSpecificText\"><\/span><span id=\"mcqSpecificCursor\" class=\"cursor mcq-specific-cursor\" style=\"display:none;\"><\/span>\r\n                  <\/span>\r\n                <\/span>\r\n              <\/div>\r\n\r\n              <div class=\"mcq-option-row\"><span class=\"mcq-radio\"><\/span><span class=\"mcq-radio-ripple\"><\/span><span class=\"mcq-option-label\">potassium chloride<\/span><\/div>\r\n              <div class=\"mcq-option-row\"><span class=\"mcq-radio\"><\/span><span class=\"mcq-radio-ripple\"><\/span><span class=\"mcq-option-label\">sodium fluoride<\/span><\/div>\r\n              <div class=\"mcq-option-row\"><span class=\"mcq-radio\"><\/span><span class=\"mcq-radio-ripple\"><\/span><span class=\"mcq-option-label\">potassium fluoride<\/span><\/div>\r\n            <\/div>\r\n\r\n            <button id=\"mcqSubmitButton\" class=\"mcq-submit-button\">Submit answer<\/button>\r\n          <\/section>\r\n\r\n          <section id=\"mcqGeneralFeedback\" class=\"mcq-general-feedback\">\r\n            <span id=\"mcqGeneralText\"><\/span><span id=\"mcqGeneralCursor\" class=\"cursor mcq-general-cursor\" style=\"display:none;\"><\/span>\r\n          <\/section>\r\n        <\/main>\r\n      <\/div>\r\n    <\/div>\r\n  <\/section>\r\n\r\n  <section id=\"sceneSaq\" class=\"ols-scene\">\r\n    <div class=\"ols-saq-stage\">\r\n      <div id=\"saqIntro\" class=\"ols-saq-intro\">\r\n        <div 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the ions can get closer together.\\n\"+\r\n\"\u2022 Smaller ions \u2192 stronger electrostatic attraction \u2192 stronger ionic lattice.\\n\"+\r\n\"\u2022 Na\u207a (0.102 nm) is smaller than K\u207a (0.138 nm).\\n\"+\r\n\"\u2022 F\u207b (0.133 nm) is smaller than Cl\u207b (0.180 nm).\\n\\n\"+\r\n\"Therefore, the strongest ionic bonding occurs in the compound formed by the smallest cation and the smallest anion \u2192 sodium fluoride (NaF).\\n\\n\"+\r\n\"The correct answer is: sodium fluoride\";\r\n\r\nconst mcqIntroScreen=document.getElementById(\"mcqIntroScreen\");\r\nconst mcqIntroTitleText=document.getElementById(\"mcqIntroTitleText\");\r\nconst mcqIntroTitleCursor=document.getElementById(\"mcqIntroTitleCursor\");\r\nconst mcqScreen=document.getElementById(\"mcqScreen\");\r\nconst mcqWrongOption=document.getElementById(\"mcqWrongOption\");\r\nconst mcqSubmitButton=document.getElementById(\"mcqSubmitButton\");\r\nconst 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because it has more atoms packed together and melts at a higher temperature than sodium.\";\r\nconst saqTeacherFeedbackText=\r\n\"Comment:\\n\"+\r\n\"This answer is not correct. Melting temperature is a result of bonding strength, not the cause of it.\\n\\n\"+\r\n\"In metallic bonding, positive metal ions are attracted to a sea of delocalised electrons. The strength of this attraction depends on the charge of the ions and the number of delocalised electrons.\\n\\n\"+\r\n\"Magnesium forms Mg\u00b2\u207a ions and contributes two delocalised electrons per atom, whereas sodium forms Na\u207a ions and contributes only one electron. This results in a stronger electrostatic attraction in magnesium. Additionally, Mg\u00b2\u207a ions have a higher charge density than Na\u207a ions, further strengthening the metallic bonding.\\n\\n\"+\r\n\"Next time, include:\\n\"+\r\n\"\u2022 Ion charge: magnesium forms Mg\u00b2\u207a, sodium forms Na\u207a \u2713\\n\"+\r\n\"\u2022 Delocalised electrons: magnesium provides more electrons to the sea \u2713\\n\"+\r\n\"\u2022 Charge density: smaller, more highly charged ions create stronger attraction \u2713\\n\\n\"+\r\n\"You were close. 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