{"id":7478,"date":"2026-09-11T17:04:57","date_gmt":"2026-09-11T16:04:57","guid":{"rendered":"https:\/\/www.onlinelearningsystem.net\/xyz\/revision-notes\/a-level-chemistry\/ocr-a\/4-1-1-basic-concepts-of-organic-chemistry\/aliphatic-alicyclic-and-aromatic-compounds\/"},"modified":"2026-09-22T09:51:51","modified_gmt":"2026-09-22T08:51:51","slug":"aliphatic-alicyclic-and-aromatic-compounds","status":"publish","type":"page","link":"https:\/\/www.onlinelearningsystem.net\/xyz\/revision-notes\/a-level-chemistry\/ocr-a\/4-1-1-basic-concepts-of-organic-chemistry\/aliphatic-alicyclic-and-aromatic-compounds\/","title":{"rendered":"Aliphatic, Alicyclic and Aromatic Compounds"},"content":{"rendered":"\n<section class=\"ols-revision-page ols-isomerism-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      --soft-yellow: #fff8e6;\n      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Chemistry<\/h4>\n    <ul class=\"ols-topic-list\">\n      <li><a href=\"https:\/\/www.onlinelearningsystem.net\/xyz\/revision-notes\/a-level-chemistry\/ocr-a\/4-1-1-basic-concepts-of-organic-chemistry\/\">Section overview<\/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\/iupac-rules\/\">IUPAC Rules<\/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\/alkene\/\">Alkene<\/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\/alcohol\/\">Alcohol<\/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\/haloalkanes\/\">Haloalkanes<\/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\/aldehyde\/\">Aldehyde<\/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\/ketone\/\">Ketone<\/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\/carboxylic-acid\/\">Carboxylic Acid<\/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\/ester\/\">Ester<\/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\/isomerism\/\">Isomerism<\/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\/aliphatic-alicyclic-and-aromatic-compounds\/\">Aliphatic, Alicyclic and Aromatic Compounds<\/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\/curly-arrows-and-mechanisms\/\">Curly Arrows and Mechanisms<\/a><\/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\/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      <li><a href=\"https:\/\/www.onlinelearningsystem.net\/xyz\/revision-notes\/a-level-chemistry\/ocr-a\/4-2-1-alcohols\/\">4.2.1 Alcohols<\/a><\/li>\n      <li><a href=\"https:\/\/www.onlinelearningsystem.net\/xyz\/revision-notes\/a-level-chemistry\/ocr-a\/4-2-2-haloalkanes\/\">4.2.2 Haloalkanes<\/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 = sidebar.querySelectorAll('a[href]');\r\n    var matched = null;\r\n    var matchedLength = 0;\r\n\r\n    sidebar.querySelectorAll('.active, .active-main, .parent-active').forEach(function(item) {\r\n      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\/\n<span>Aliphatic, Alicyclic and Aromatic Compounds<\/span>\n<\/nav>\n\n      <header class=\"ols-title-card\">\n        <h1>Aliphatic, Alicyclic and Aromatic Compounds<\/h1>\n        <p class=\"ols-page-intro\">A concise OCR A Level Chemistry A revision guide to the terms used to classify organic compounds in 4.1.1(c): aliphatic, alicyclic and aromatic, and the full OCR meaning of saturated and unsaturated, which includes triple bonds and benzene rings.<\/p>\n\n        <div class=\"ols-badges\">\n          <div class=\"ols-badge\">Paper 2<\/div>\n<div class=\"ols-badge\">4.1.1: Basic Concepts of Organic Chemistry<\/div>\n<div class=\"ols-badge\">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: Saturated and Unsaturated Hydrocarbons<\/h2>\n<p>Before you meet the new words, check what you already know about saturated and unsaturated hydrocarbons.<\/p>\n<div class=\"ols-h5p-frame\"><div class=\"h5p-content\" data-content-id=\"796\"><\/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>Three Families of Organic Compound<\/h2>\n<\/div>\n<p>OCR groups every organic compound into one of three families according to the shape of its carbon skeleton. The terms appear in exam questions as instructions (&#8220;draw an alicyclic isomer&#8221;) and as definitions to state, so learn the wording exactly.<\/p>\n<div class=\"ols-table-wrap\">\n<table class=\"ols-table\">\n<thead>\n<tr><th>Term<\/th><th>OCR definition<\/th><th>Examples<\/th><\/tr>\n<\/thead>\n<tbody>\n<tr><td><strong>Aliphatic<\/strong><\/td><td>A compound containing carbon and hydrogen joined together in straight chains, branched chains or non-aromatic rings<\/td><td>Butane, 2-methylpropane, cyclohexane, ethanol<\/td><\/tr>\n<tr><td><strong>Alicyclic<\/strong><\/td><td>An aliphatic compound arranged in non-aromatic rings, with or without side chains<\/td><td>Cyclohexane, cyclopentene, methylcyclohexane<\/td><\/tr>\n<tr><td><strong>Aromatic<\/strong><\/td><td>A compound containing a benzene ring<\/td><td>Benzene, methylbenzene, phenol<\/td><\/tr>\n<\/tbody>\n<\/table>\n<\/div>\n<p>Notice that <strong>alicyclic compounds are a subset of aliphatic compounds<\/strong>: a ring that is not a benzene ring is aliphatic and alicyclic at the same time. The only compounds that are not aliphatic are the aromatic ones.<\/p>\n<div class=\"ols-figure-card ols-zoom-pop\">\n<div class=\"ols-figure-image\">\n<a class=\"ols-image-fullscreen-link\" href=\"https:\/\/www.onlinelearningsystem.net\/xyz\/wp-content\/uploads\/2026\/09\/hexane-cyclohexane-methylbenzene.jpg\" target=\"_blank\" rel=\"noopener\" aria-label=\"Open image fullscreen\">\n<img decoding=\"async\" src=\"https:\/\/www.onlinelearningsystem.net\/xyz\/wp-content\/uploads\/2026\/09\/hexane-cyclohexane-methylbenzene.jpg\" alt=\"Hexane (aliphatic), cyclohexane (alicyclic) and methylbenzene (aromatic) skeletal formulae\" data-fullscreen-src=\"https:\/\/www.onlinelearningsystem.net\/xyz\/wp-content\/uploads\/2026\/09\/hexane-cyclohexane-methylbenzene.jpg\">\n<\/a>\n<\/div>\n<div class=\"ols-figure-caption\"><p>The three families: hexane is aliphatic, cyclohexane is alicyclic (and therefore aliphatic), methylbenzene is aromatic.<\/p><\/div>\n<\/div>\n<div class=\"ols-key-box\">\n<p><strong>Exam sentence:<\/strong> An alicyclic compound contains carbon atoms arranged in a non-aromatic ring; an aromatic compound contains a benzene ring.<\/p>\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: Put Three New Compounds in a Family<\/h2>\n<p>Drag the words into the gaps to classify three compounds that are not used above.<\/p>\n<div class=\"ols-h5p-frame\"><div class=\"h5p-iframe-wrapper\"><iframe id=\"h5p-iframe-394\" class=\"h5p-iframe\" data-content-id=\"394\" style=\"height:1px\" src=\"about:blank\" frameBorder=\"0\" scrolling=\"no\" title=\"Aliphatic and Aromatic Drag: Placing Three New Compounds in a Family\"><\/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: Which One Is Alicyclic?<\/h2>\n<p>Only one of these four compounds has its carbon atoms in a non-aromatic ring.<\/p>\n<div class=\"ols-h5p-frame\"><div class=\"h5p-iframe-wrapper\"><iframe id=\"h5p-iframe-395\" class=\"h5p-iframe\" data-content-id=\"395\" style=\"height:1px\" src=\"about:blank\" frameBorder=\"0\" scrolling=\"no\" title=\"Aliphatic and Aromatic MCQ: Which of These Four Is Alicyclic?\"><\/iframe><\/div><\/div>\n<\/section>\n<article class=\"ols-note-card\">\n<div class=\"ols-note-title\">\n<div class=\"ols-note-icon\">2<\/div>\n<h2>Saturated and Unsaturated: The OCR Wording<\/h2>\n<\/div>\n<p>Most courses define an unsaturated compound as one with a C=C double bond. OCR uses a wider definition that you must reproduce in full:<\/p>\n<ul>\n<li><strong>Saturated:<\/strong> single carbon-carbon bonds only.<\/li>\n<li><strong>Unsaturated:<\/strong> the presence of multiple carbon-carbon bonds, including <strong>C=C<\/strong>, <strong>C&#8801;C<\/strong> and <strong>aromatic rings<\/strong>.<\/li>\n<\/ul>\n<div class=\"ols-table-wrap\">\n<table class=\"ols-table\">\n<thead>\n<tr><th>Compound<\/th><th>Carbon-carbon bonds present<\/th><th>Saturated or unsaturated?<\/th><th>Family<\/th><\/tr>\n<\/thead>\n<tbody>\n<tr><td><strong>Propane<\/strong><\/td><td>Single only<\/td><td>Saturated<\/td><td>Aliphatic<\/td><\/tr>\n<tr><td><strong>Cyclopentane<\/strong><\/td><td>Single only (in a ring)<\/td><td>Saturated<\/td><td>Alicyclic<\/td><\/tr>\n<tr><td><strong>But-2-ene<\/strong><\/td><td>One C=C<\/td><td>Unsaturated<\/td><td>Aliphatic<\/td><\/tr>\n<tr><td><strong>Cyclohexene<\/strong><\/td><td>One C=C in a ring<\/td><td>Unsaturated<\/td><td>Alicyclic<\/td><\/tr>\n<tr><td><strong>Ethyne<\/strong><\/td><td>One C&#8801;C<\/td><td>Unsaturated<\/td><td>Aliphatic<\/td><\/tr>\n<tr><td><strong>Benzene<\/strong><\/td><td>Delocalised aromatic ring<\/td><td>Unsaturated<\/td><td>Aromatic<\/td><\/tr>\n<\/tbody>\n<\/table>\n<\/div>\n<div class=\"ols-key-box\">\n<p><strong>Exam focus:<\/strong> A ring on its own does not make a compound unsaturated. Cyclohexane is saturated; cyclohexene and benzene are unsaturated. Saturation is about the carbon-carbon bond order, not about whether there is a ring.<\/p>\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: Spot the Unsaturated Compounds<\/h2>\n<p>Click every compound in the list that is unsaturated, using the full definition.<\/p>\n<div class=\"ols-h5p-frame\"><div class=\"h5p-iframe-wrapper\"><iframe id=\"h5p-iframe-396\" class=\"h5p-iframe\" data-content-id=\"396\" style=\"height:1px\" src=\"about:blank\" frameBorder=\"0\" scrolling=\"no\" title=\"Aliphatic and Aromatic Mark the Words: Which of These Are Unsaturated?\"><\/iframe><\/div><\/div>\n<\/section>\n<article class=\"ols-note-card purple\">\n<div class=\"ols-note-title\">\n<div class=\"ols-note-icon\">3<\/div>\n<h2>Why the Classification Matters<\/h2>\n<\/div>\n<p>The family a compound belongs to predicts how it reacts, which is why OCR introduces the terms before any reactions are studied.<\/p>\n<div class=\"ols-table-wrap\">\n<table class=\"ols-table\">\n<thead>\n<tr><th>Family<\/th><th>Typical reactivity<\/th><th>Where you meet it<\/th><\/tr>\n<\/thead>\n<tbody>\n<tr><td><strong>Saturated aliphatic (alkanes, cycloalkanes)<\/strong><\/td><td>Unreactive; only radical substitution and combustion<\/td><td>4.1.2 Alkanes<\/td><\/tr>\n<tr><td><strong>Unsaturated aliphatic (alkenes)<\/strong><\/td><td>Electrophilic addition across the \u03c0 bond<\/td><td>4.1.3 Alkenes<\/td><\/tr>\n<tr><td><strong>Aromatic (benzene and its derivatives)<\/strong><\/td><td>Electrophilic substitution, not addition, because the delocalised ring is stable<\/td><td>6.1.1 Aromatic compounds (A Level)<\/td><\/tr>\n<\/tbody>\n<\/table>\n<\/div>\n<p>The bromine water test illustrates the difference. An unsaturated aliphatic compound such as cyclohexene decolourises bromine water at once, but benzene, although unsaturated, does not react under the same conditions because addition would destroy its stable delocalised ring.<\/p>\n<div class=\"ols-key-box\">\n<p><strong>Key idea:<\/strong> Classify first, then predict: saturated aliphatic compounds substitute, unsaturated aliphatic compounds add, aromatic compounds substitute while keeping the ring.<\/p>\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: Predict What Each Compound Does<\/h2>\n<p>In each round, choose the one statement that is accurate.<\/p>\n<div class=\"ols-h5p-frame\"><div class=\"h5p-iframe-wrapper\"><iframe id=\"h5p-iframe-397\" class=\"h5p-iframe\" data-content-id=\"397\" style=\"height:1px\" src=\"about:blank\" frameBorder=\"0\" scrolling=\"no\" title=\"Aliphatic and Aromatic Summary: Predicting Reactions from the Family\"><\/iframe><\/div><\/div>\n<\/section>\n<article class=\"ols-note-card soft\">\n<div class=\"ols-note-title\">\n<div class=\"ols-note-icon\">4<\/div>\n<h2>Common Exam Mistakes<\/h2>\n<\/div>\n<ul>\n<li>Calling cyclohexane &#8220;aromatic&#8221; because it is a six-membered ring. Aromatic means it contains a <strong>benzene<\/strong> ring.<\/li>\n<li>Saying an alicyclic compound is not aliphatic. Alicyclic compounds are aliphatic compounds in rings.<\/li>\n<li>Defining unsaturated as &#8220;contains a C=C bond&#8221; only. OCR also includes C&#8801;C and aromatic rings.<\/li>\n<li>Describing a cycloalkane as unsaturated because it has &#8220;fewer hydrogens than the alkane&#8221;. 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background 0.25s ease,\r\n        color 0.25s ease;\r\n    }\r\n\r\n    .ols-course-cta-alkenes .ols-animation-start-overlay:hover .ols-animation-play-circle {\r\n      transform: scale(1.08);\r\n      background: var(--navy);\r\n      color: #ffffff;\r\n    }\r\n\r\n    .ols-course-cta-alkenes .ols-animation-play-icon {\r\n      width: 0;\r\n      height: 0;\r\n      margin-left: 7px;\r\n      border-top: 18px solid transparent;\r\n      border-bottom: 18px solid transparent;\r\n      border-left: 28px solid currentColor;\r\n    }\r\n\r\n    .ols-course-cta-alkenes .ols-animation-start-text {\r\n      max-width: 540px;\r\n      margin: 0;\r\n      color: #ffffff;\r\n      font-size: clamp(20px, 3vw, 32px);\r\n      line-height: 1.2;\r\n      font-weight: 800;\r\n      text-shadow: 0 8px 20px rgba(0, 0, 0, 0.28);\r\n    }\r\n\r\n    .ols-course-cta-alkenes .ols-animation-pause-button {\r\n      position: absolute;\r\n      left: 16px;\r\n      bottom: 16px;\r\n      z-index: 7;\r\n      display: none;\r\n      align-items: center;\r\n      justify-content: center;\r\n      min-width: 92px;\r\n      padding: 10px 16px;\r\n      border: 0;\r\n      border-radius: 999px;\r\n      background: rgba(28, 36, 75, 0.92);\r\n      color: #ffffff;\r\n      font-family: Poppins, Arial, sans-serif;\r\n      font-size: 14px;\r\n      line-height: 1.2;\r\n      font-weight: 800;\r\n      cursor: pointer;\r\n      box-shadow: 0 12px 28px rgba(28, 36, 75, 0.24);\r\n      transition:\r\n        transform 0.2s ease,\r\n        background 0.2s ease,\r\n        box-shadow 0.2s ease;\r\n    }\r\n\r\n    .ols-course-cta-alkenes .ols-animation-pause-button:hover {\r\n      transform: translateY(-2px);\r\n      background: var(--blue);\r\n      box-shadow: 0 16px 34px rgba(37, 99, 235, 0.28);\r\n    }\r\n\r\n    .ols-course-cta-alkenes .ols-animation-pause-button.is-visible {\r\n      display: inline-flex;\r\n    }\r\n\r\n    @keyframes olsAnimationPlayPulse001 {\r\n      0% {\r\n        box-shadow:\r\n          0 18px 40px rgba(28, 36, 75, 0.30),\r\n          0 0 0 0 rgba(255, 255, 255, 0.40);\r\n      }\r\n\r\n      70% {\r\n        box-shadow:\r\n          0 18px 40px rgba(28, 36, 75, 0.30),\r\n          0 0 0 18px rgba(255, 255, 255, 0);\r\n      }\r\n\r\n      100% {\r\n        box-shadow:\r\n          0 18px 40px rgba(28, 36, 75, 0.30),\r\n          0 0 0 0 rgba(255, 255, 255, 0);\r\n      }\r\n    }\r\n\r\n    .ols-course-cta-alkenes .ols-course-video-status {\r\n      margin: 14px 0 0;\r\n      text-align: center;\r\n      color: var(--grey-text);\r\n      font-size: 13px;\r\n      line-height: 1.5;\r\n      font-weight: 500;\r\n    }\r\n\r\n    .ols-course-cta-alkenes .ols-course-cta-bottom {\r\n      display: flex;\r\n      justify-content: center;\r\n      padding-top: 22px;\r\n      border-top: 1px solid var(--border);\r\n    }\r\n\r\n    .ols-course-cta-alkenes .ols-course-button {\r\n      display: inline-flex;\r\n      align-items: center;\r\n      justify-content: center;\r\n      padding: 15px 28px;\r\n      border-radius: 999px;\r\n      background: var(--navy);\r\n      color: #ffffff;\r\n      text-decoration: none;\r\n      font-size: 16px;\r\n      line-height: 1.2;\r\n      font-weight: 800;\r\n      box-shadow: 0 12px 26px rgba(28, 36, 75, 0.18);\r\n      transition:\r\n        transform 0.2s ease,\r\n        background 0.2s ease,\r\n        box-shadow 0.2s ease;\r\n    }\r\n\r\n    .ols-course-cta-alkenes .ols-course-button:hover {\r\n      transform: translateY(-2px);\r\n      background: var(--blue);\r\n      color: #ffffff;\r\n      box-shadow: 0 16px 32px rgba(37, 99, 235, 0.24);\r\n    }\r\n\r\n    .ols-course-cta-alkenes .ols-course-button-top {\r\n      flex-shrink: 0;\r\n      padding: 12px 22px;\r\n      font-size: 15px;\r\n    }\r\n\r\n    @media (max-width: 900px) {\r\n      .ols-course-cta-alkenes .ols-course-cta-top {\r\n        grid-template-columns: 1fr;\r\n      }\r\n\r\n      .ols-course-cta-alkenes .ols-course-cta-image-link {\r\n        max-width: 520px;\r\n        margin: 0 auto;\r\n      }\r\n\r\n      .ols-course-cta-alkenes .ols-course-cta-intro-stats {\r\n        grid-template-columns: 1fr;\r\n      }\r\n\r\n      .ols-course-cta-alkenes .ols-animation-frame-shell {\r\n        height: 520px;\r\n      }\r\n    }\r\n\r\n    @media (max-width: 760px) {\r\n      .ols-course-cta-alkenes {\r\n        margin: 26px 0 22px;\r\n      }\r\n\r\n      .ols-course-cta-alkenes .ols-course-cta-card {\r\n        padding: 20px;\r\n        border-radius: 24px;\r\n      }\r\n\r\n      .ols-course-cta-alkenes .ols-course-cta-header-row {\r\n        align-items: stretch;\r\n      }\r\n\r\n      .ols-course-cta-alkenes .ols-course-button-top {\r\n        width: 100%;\r\n      }\r\n\r\n      .ols-course-cta-alkenes .ols-course-cta-stats,\r\n      .ols-course-cta-alkenes .ols-course-cta-features {\r\n        grid-template-columns: 1fr;\r\n      }\r\n\r\n      .ols-course-cta-alkenes .ols-course-animation-wrap {\r\n        padding: 0;\r\n        border-radius: 0;\r\n      }\r\n\r\n      .ols-course-cta-alkenes .ols-animation-frame-shell {\r\n        height: 420px;\r\n        border-radius: 18px;\r\n      }\r\n\r\n      .ols-course-cta-alkenes .ols-animation-play-circle {\r\n        width: 76px;\r\n        height: 76px;\r\n      }\r\n\r\n      .ols-course-cta-alkenes .ols-animation-play-icon {\r\n        border-top-width: 14px;\r\n        border-bottom-width: 14px;\r\n        border-left-width: 22px;\r\n      }\r\n\r\n      .ols-course-cta-alkenes .ols-animation-pause-button {\r\n        left: 12px;\r\n        bottom: 12px;\r\n        min-width: 84px;\r\n        padding: 9px 14px;\r\n        font-size: 13px;\r\n      }\r\n\r\n      .ols-course-cta-alkenes .ols-course-button {\r\n        width: 100%;\r\n      }\r\n    }\r\n  <\/style>\r\n\r\n  <div class=\"ols-course-cta-card\">\r\n\r\n    <div class=\"ols-course-cta-top\">\r\n\r\n      <a class=\"ols-course-cta-image-link\" href=\"https:\/\/www.onlinelearningsystem.net\/xyz\/product\/basic-concepts-of-organic-chemistry-and-alkanes-4-1-1-4-1-2-ocr-a\/\" aria-label=\"Open the OCR A Level Chemistry A 4.1.1 and 4.1.2 Basic Concepts of Organic Chemistry and Alkanes 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-4-1-1-4-1-2-organic-chemistry-alkanes-interactive-course-banner.jpg\"\r\n            alt=\"OCR A Level Chemistry A 4.1.3 Basic Concepts of Organic Chemistry and Alkanes 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 | 4.1.1 and 4.1.2 Course\r\n          <\/div>\r\n\r\n          <a class=\"ols-course-button ols-course-button-top\" href=\"https:\/\/www.onlinelearningsystem.net\/xyz\/product\/basic-concepts-of-organic-chemistry-and-alkanes-4-1-1-4-1-2-ocr-a\/\">\r\n            View Course\r\n          <\/a>\r\n\r\n        <\/div>\r\n\r\n        <h2>\r\n          Master Basic Concepts of Organic Chemistry and Alkanes 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 4.1.1 and 4.1.2 Basic Concepts of Organic Chemistry and Alkanes 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 4.1.1 and 4.1.2 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\/basic-concepts-of-organic-chemistry-and-alkanes-4-1-1-4-1-2-ocr-a\/\">\r\n        View Basic Concepts of Organic Chemistry and Alkanes 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  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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  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<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 class=\"ols-saq-intro-title-wrap\">\r\n          <h1 class=\"ols-saq-intro-title\">\r\n            <span id=\"saqIntroTitleText\"><\/span><span id=\"saqIntroTitleCursor\" class=\"ols-title-cursor\"><\/span>\r\n          <\/h1>\r\n        <\/div>\r\n      <\/div>\r\n\r\n      <div class=\"ols-saq-scale-wrap\">\r\n        <main id=\"saqScreen\" class=\"ols-saq-screen\">\r\n          <section class=\"saq-question-area\">\r\n            <div class=\"saq-question-text\">\r\n              <strong>(ii)<\/strong>&nbsp;&nbsp; Melting temperature depends on the strength of metallic bonding.<br>\r\n              Explain why the metallic bonding in magnesium is much stronger than that in sodium.\r\n            <\/div>\r\n\r\n            <div class=\"saq-student-box\">\r\n              <span id=\"saqStudentText\"><\/span><span id=\"saqStudentCursor\" class=\"cursor\"><\/span>\r\n            <\/div>\r\n          <\/section>\r\n\r\n          <section id=\"saqTeacherFeedback\" 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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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