{"id":12364,"date":"2026-09-30T19:39:56","date_gmt":"2026-09-30T18:39:56","guid":{"rendered":"https:\/\/www.onlinelearningsystem.net\/xyz\/revision-notes\/a-level-chemistry\/aqa\/3-1-9-rate-equations\/the-iodine-propanone-reaction\/"},"modified":"2026-10-03T11:51:26","modified_gmt":"2026-10-03T10:51:26","slug":"the-iodine-propanone-reaction","status":"publish","type":"page","link":"https:\/\/www.onlinelearningsystem.net\/xyz\/revision-notes\/a-level-chemistry\/aqa\/3-1-9-rate-equations\/the-iodine-propanone-reaction\/","title":{"rendered":"The Iodine\u2013Propanone Reaction"},"content":{"rendered":"\n<section class=\"ols-revision-page ols-nature-of-covalent-bonding-9ch0-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-orange: #fff7ed;\n      --grey-text: #667085;\n      --body-text: #1f2937;\n      --border: rgba(28, 36, 75, 0.14);\n      --shadow: 0 18px 45px rgba(28, 36, 75, 0.10);\n      --inner-shadow: 0 10px 26px rgba(28, 36, 75, 0.08);\n      font-family: Poppins, Arial, sans-serif;\n      color: var(--navy);\n      background: #ffffff;\n    }\n\n    .ols-revision-page * { box-sizing: border-box; }\n    .ols-main { min-width: 0; max-width: 970px; }\n    .ols-breadcrumbs { display: flex; flex-wrap: wrap; gap: 8px; margin: 10px 0 22px; font-size: 15px; color: var(--grey-text); }\n    .ols-breadcrumbs a, .ols-breadcrumbs span { color: var(--grey-text); text-decoration: none; font-weight: 600; }\n    .ols-breadcrumbs a:hover { color: var(--blue); text-decoration: underline; text-underline-offset: 3px; }\n    .ols-title-card, .ols-note-card, .ols-h5p-card, .ols-related-card, .ols-faq-card { background: #ffffff; border: 1px solid var(--border); border-radius: 28px; box-shadow: var(--shadow); padding: 34px; margin-bottom: 24px; overflow: hidden; }\n    .ols-title-card { background: linear-gradient(135deg, #ffffff 0%, #f8fbff 100%); }\n    .ols-title-card h1 { margin: 0 0 18px; font-size: clamp(36px, 5vw, 58px); line-height: 1.08; font-weight: 800; letter-spacing: -0.04em; color: #111827; }\n    .ols-page-intro { font-size: 19px; line-height: 1.7; font-weight: 300; color: var(--body-text); margin: 0 0 22px; }\n    .ols-badges { display: flex; flex-direction: column; align-items: flex-start; gap: 12px; margin-bottom: 22px; }\n    .ols-badge { display: inline-flex; align-items: center; padding: 9px 14px; border-radius: 999px; background: #ffffff; border: 1px solid var(--border); font-size: 15px; font-weight: 600; color: var(--navy); }\n    .ols-author { display: flex; align-items: center; gap: 20px; padding: 28px; border-radius: 28px; background: linear-gradient(135deg, #ffffff 0%, #f8fbff 100%); border: 1px solid rgba(28,36,75,0.12); box-shadow: 0 18px 45px rgba(28,36,75,0.10); margin-top: 22px; }\n    .ols-author-avatar-img { width: 92px; height: 92px; border-radius: 50%; object-fit: cover; object-position: center; flex-shrink: 0; border: 4px solid #ffffff; box-shadow: 0 14px 32px rgba(28,36,75,0.18), 0 0 0 1px rgba(28,36,75,0.10); transition: transform 0.25s ease, box-shadow 0.25s ease; }\n    .ols-author:hover .ols-author-avatar-img { transform: scale(1.04); box-shadow: 0 20px 42px rgba(28,36,75,0.22), 0 0 0 1px rgba(28,36,75,0.10); }\n    .ols-author-content { min-width: 0; }\n    .ols-author-title { margin: 0 0 4px; font-size: clamp(24px,3vw,34px); line-height: 1.15; font-weight: 700; color: var(--navy); letter-spacing: -0.03em; }\n    .ols-author-description { margin: 0; font-size: 17px; line-height: 1.7; font-weight: 300; color: var(--grey-text); }\n    .ols-linkedin-pill { display: inline-flex; align-items: center; justify-content: center; gap: 10px; margin-top: 16px; padding: 11px 18px; border-radius: 999px; background: linear-gradient(135deg,#0A66C2,#004182); color: #ffffff; text-decoration: none; font-size: 14px; line-height: 1; font-weight: 700; letter-spacing: 0.01em; box-shadow: 0 10px 22px rgba(10,102,194,0.24); position: relative; overflow: hidden; transition: transform 0.22s ease, box-shadow 0.22s ease; }\n    .ols-linkedin-pill::before { content: \"\"; position: absolute; top: 0; left: -120%; width: 100%; height: 100%; background: linear-gradient(120deg, rgba(255,255,255,0) 0%, rgba(255,255,255,0.28) 50%, rgba(255,255,255,0) 100%); transition: left 0.7s ease; }\n    .ols-linkedin-pill:hover { transform: translateY(-3px) scale(1.03); box-shadow: 0 16px 34px rgba(10,102,194,0.34), 0 0 0 6px rgba(10,102,194,0.10); color: #ffffff; }\n    .ols-linkedin-pill:hover::before { left: 120%; }\n    .ols-linkedin-icon { width: 18px; height: 18px; display: block; flex-shrink: 0; }\n\n    .ols-note-card.soft { background: linear-gradient(135deg, #ffffff 0%, var(--soft-red) 100%); }\n    .ols-note-card.purple { background: linear-gradient(135deg, #ffffff 0%, var(--soft-purple) 100%); }\n    .ols-note-card.orange { background: linear-gradient(135deg, #ffffff 0%, var(--soft-orange) 100%); }\n    .ols-note-title { display: flex; align-items: center; gap: 14px; margin-bottom: 20px; }\n    .ols-note-icon { width: 52px; height: 52px; border-radius: 16px; background: var(--navy); color: #ffffff; display: grid; place-items: center; font-size: 24px; font-weight: 800; flex-shrink: 0; }\n    .ols-note-title h2, .ols-h5p-card h2, .ols-related-card h2, .ols-faq-card h2 { margin: 0; font-size: clamp(28px, 3.5vw, 42px); line-height: 1.15; font-weight: 800; color: #111827; letter-spacing: -0.03em; }\n    .ols-h5p-card h2, .ols-related-card h2, .ols-faq-card h2 { margin-bottom: 14px; }\n    .ols-note-card p, .ols-note-card li { font-size: clamp(15px, 1.25vw, 17px); line-height: 1.65; font-weight: 300; color: var(--body-text); }\n    .ols-h5p-card p, .ols-related-card p, .ols-faq-card p { font-size: clamp(15px, 1.3vw, 18px); line-height: 1.65; font-weight: 300; color: var(--body-text); }\n    .ols-note-card strong, .ols-h5p-card strong, .ols-related-card strong, .ols-faq-card strong { font-weight: 700; color: var(--navy); }\n    .ols-note-card ul, .ols-note-card ol { margin: 0; padding-left: 22px; }\n\n    .ols-key-box { margin-top: 20px; background: var(--soft-green); border: 1px solid rgba(63, 143, 70, 0.25); border-radius: 20px; padding: 18px 20px; }\n    .ols-key-box p { margin: 0; font-weight: 400; color: var(--navy); }\n    .ols-definition-box { background: linear-gradient(135deg, #ffffff, var(--soft-purple)); border: 2px dashed rgba(122, 62, 157, 0.35); border-radius: 24px; padding: 22px 24px; margin-top: 22px; }\n    .ols-definition-box p { margin: 0; color: var(--navy); font-weight: 400; }\n\n    .ols-rule-list { display: grid; gap: 14px; margin-top: 18px; }\n    .ols-rule-item { background: #ffffff; border: 1px solid var(--border); border-left: 5px solid var(--blue); border-radius: 18px; padding: 18px; box-shadow: var(--inner-shadow); }\n    .ols-rule-item h3 { margin: 0 0 8px; font-size: 20px; line-height: 1.25; color: var(--navy); }\n    .ols-rule-item p { margin: 0; font-size: 15px; line-height: 1.6; }\n\n    .ols-figure-card { margin: 26px auto 4px; border: 1px solid var(--border); border-radius: 26px; overflow: hidden; background: #ffffff; box-shadow: var(--inner-shadow); max-width: 100%; }\n    .ols-figure-card.medium { max-width: 820px; }\n    .ols-figure-card.compact { max-width: 700px; }\n    .ols-figure-image { width: 100%; min-height: 260px; display: flex; align-items: center; justify-content: center; background: #ffffff; padding: 20px; }\n    .ols-figure-image img { max-width: 100%; height: auto; display: block; }\n    .ols-figure-caption { padding: 18px 24px 22px; background: linear-gradient(135deg, #ffffff, #f8fbff); border-top: 1px solid var(--border); }\n    .ols-figure-caption p { margin: 0; color: #5f6b85; font-size: clamp(15px, 1.3vw, 17px); line-height: 1.6; font-weight: 300; font-style: italic; }\n    .ols-zoom-card, .ols-zoom-card * { box-sizing: border-box; }\n    .ols-zoom-card { display: block !important; margin: 26px auto 34px !important; border: 1px solid rgba(28, 36, 75, 0.14) !important; border-radius: 26px !important; background: #ffffff !important; box-shadow: 0 18px 45px rgba(28, 36, 75, 0.10) !important; overflow: visible !important; position: relative !important; z-index: 1 !important; isolation: isolate !important; }\n    .ols-zoom-card.medium { max-width: 820px; }\n    .ols-zoom-card.compact { max-width: 700px; }\n    .ols-zoom-card.wide { max-width: 940px; }\n    .ols-zoom-card.slim { max-width: 600px; }\n    .ols-zoom-card:hover { z-index: 50 !important; }\n    .ols-zoom-card-image { display: flex !important; align-items: center !important; justify-content: center !important; width: 100% !important; min-height: 240px !important; padding: 20px !important; background: #ffffff !important; overflow: visible !important; border-top-left-radius: 26px !important; border-top-right-radius: 26px !important; position: relative !important; z-index: 2 !important; }\n    .ols-zoom-card img.ols-zoomable-img { display: block !important; max-width: 100% !important; height: auto !important; border-radius: 18px !important; cursor: zoom-in !important; pointer-events: auto !important; user-select: none !important; -webkit-user-drag: none !important; transform: translateZ(0) scale(1) !important; transform-origin: center center !important; transition: transform 0.32s ease, box-shadow 0.32s ease, filter 0.32s ease !important; position: relative !important; z-index: 2 !important; }\n    @media (hover: hover) and (pointer: fine) { .ols-zoom-card img.ols-zoomable-img:hover { transform: translateZ(0) scale(1.35) !important; box-shadow: 0 28px 70px rgba(28, 36, 75, 0.34) !important; filter: saturate(1.02) contrast(1.01) !important; z-index: 100 !important; } }\n    .ols-zoom-card-caption { padding: 18px 22px 20px !important; background: linear-gradient(135deg, #ffffff, #f8fbff) !important; border-bottom-left-radius: 26px !important; border-bottom-right-radius: 26px !important; position: relative !important; z-index: 1 !important; }\n    .ols-zoom-card-caption p { margin: 0 !important; color: #5f6b85 !important; font-size: 15px !important; line-height: 1.65 !important; font-weight: 300 !important; font-style: italic !important; font-family: Poppins, Arial, sans-serif !important; }\n    .ols-image-lightbox { position: fixed; inset: 0; z-index: 999999; display: none; align-items: center; justify-content: center; padding: 34px; background: rgba(10, 15, 35, 0.86); backdrop-filter: blur(8px); -webkit-backdrop-filter: blur(8px); }\n    .ols-image-lightbox.is-open { display: flex; }\n    .ols-image-lightbox-inner { position: relative; width: min(96vw, 1500px); max-height: 92vh; display: flex; align-items: center; justify-content: center; }\n    .ols-image-lightbox-img { display: block; max-width: 100%; max-height: 92vh; height: auto; width: auto; border-radius: 22px; background: #ffffff; box-shadow: 0 32px 90px rgba(0, 0, 0, 0.45); object-fit: contain; }\n    .ols-image-lightbox-close { position: absolute; top: -18px; right: -18px; width: 46px; height: 46px; border: 0; border-radius: 50%; background: #ffffff; color: var(--navy); font-family: Poppins, Arial, sans-serif; font-size: 28px; line-height: 1; font-weight: 700; cursor: pointer; box-shadow: 0 16px 34px rgba(0, 0, 0, 0.28); display: flex; align-items: center; justify-content: center; transition: transform 0.2s ease, background 0.2s ease, color 0.2s ease; }\n    .ols-image-lightbox-close:hover { transform: scale(1.08); background: var(--blue); color: #ffffff; }\n    @media (max-width: 760px) { .ols-zoom-card { border-radius: 22px !important; overflow: hidden !important; } .ols-zoom-card-image { min-height: auto !important; padding: 12px !important; overflow: hidden !important; border-top-left-radius: 22px !important; border-top-right-radius: 22px !important; } .ols-zoom-card img.ols-zoomable-img, .ols-zoom-card img.ols-zoomable-img:hover { transform: none !important; box-shadow: none !important; } .ols-zoom-card-caption { border-bottom-left-radius: 22px !important; border-bottom-right-radius: 22px !important; } .ols-image-lightbox { padding: 16px; } .ols-image-lightbox-inner { width: 100%; max-height: 88vh; } .ols-image-lightbox-img { max-height: 88vh; border-radius: 16px; } .ols-image-lightbox-close { top: 10px; right: 10px; width: 42px; height: 42px; font-size: 26px; } }\n\n\n    .ols-table-wrap { overflow: hidden; border-radius: 22px; border: 1px solid var(--border); background: #ffffff; margin-top: 18px; }\n    .ols-table { width: 100%; border-collapse: collapse; table-layout: fixed; }\n    .ols-table th { background: var(--navy); color: #ffffff; padding: 16px; text-align: left; font-size: clamp(14px, 1.2vw, 17px); font-weight: 600; overflow-wrap: anywhere; }\n    .ols-table td { padding: 16px; border-bottom: 1px solid var(--border); font-size: clamp(14px, 1.15vw, 16px); line-height: 1.45; color: var(--body-text); vertical-align: top; overflow-wrap: anywhere; }\n    .ols-table tr:last-child td { border-bottom: none; }\n\n    .ols-h5p-card { background: linear-gradient(135deg, #ffffff 0%, #f7f0ff 100%); }\n    .ols-h5p-frame { margin-top: 22px; padding: 18px; border-radius: 24px; background: #ffffff; border: 1px solid var(--border); box-shadow: inset 0 0 0 1px rgba(28, 36, 75, 0.03); }\n\n    .ols-faq-list { display: grid; gap: 14px; margin-top: 18px; }\n    .ols-faq-item { background: #ffffff; border: 1px solid var(--border); border-radius: 18px; padding: 18px 20px; box-shadow: var(--inner-shadow); }\n    .ols-faq-item h3 { margin: 0 0 8px; font-size: 20px; line-height: 1.3; color: var(--navy); }\n    .ols-faq-item p { margin: 0; font-size: 16px; line-height: 1.65; color: var(--body-text); }\n\n    .ols-related-grid { display: grid; grid-template-columns: repeat(3, minmax(0, 1fr)); gap: 16px; margin-top: 18px; }\n    .ols-related-item { border: 1px solid var(--border); border-radius: 18px; padding: 18px; background: #ffffff; color: var(--navy); text-decoration: none; font-weight: 600; line-height: 1.5; transition: transform 0.2s ease, box-shadow 0.2s ease; }\n    .ols-related-item:hover { transform: translateY(-2px); box-shadow: 0 10px 22px rgba(28, 36, 75, 0.08); }\n\n    .ols-course-cta-covalent {\n      width: 100%;\n      margin: 30px 0 24px;\n      font-family: Poppins, Arial, sans-serif;\n    }\n    .ols-course-cta-covalent, .ols-course-cta-covalent * { box-sizing: border-box; }\n    .ols-course-cta-card {\n      overflow: hidden;\n      border-radius: 30px;\n      border: 1px solid var(--border);\n      background: radial-gradient(circle at top left, rgba(37, 99, 235, 0.16), transparent 34%), linear-gradient(135deg, #ffffff 0%, #f8fbff 100%);\n      box-shadow: var(--shadow);\n      padding: 30px;\n    }\n    .ols-course-cta-top {\n      display: grid;\n      grid-template-columns: minmax(260px, 0.9fr) minmax(0, 1.1fr);\n      gap: 28px;\n      align-items: center;\n      margin-bottom: 24px;\n    }\n    .ols-course-cta-image-link { display: block; text-decoration: none; border-radius: 24px; }\n    .ols-course-cta-image {\n      width: 100%;\n      border-radius: 24px;\n      overflow: hidden;\n      border: 1px solid var(--border);\n      background: #ffffff;\n      box-shadow: var(--inner-shadow);\n      transition: transform 0.35s ease, box-shadow 0.35s ease;\n    }\n    .ols-course-cta-image img { width: 100%; height: auto; display: block; transition: transform 0.45s ease; }\n    .ols-course-cta-image-link:hover .ols-course-cta-image { transform: translateY(-8px) scale(1.015); box-shadow: 0 26px 60px rgba(28, 36, 75, 0.18), 0 0 0 1px rgba(37, 99, 235, 0.12); }\n    .ols-course-cta-image-link:hover .ols-course-cta-image img { transform: scale(1.03); }\n    .ols-course-cta-header-row { display: flex; flex-wrap: wrap; align-items: center; justify-content: space-between; gap: 14px; margin-bottom: 18px; }\n    .ols-course-cta-kicker { display: inline-flex; align-items: center; padding: 8px 14px; border-radius: 999px; background: #ffffff; border: 1px solid rgba(37, 99, 235, 0.18); color: var(--blue); font-size: 14px; line-height: 1.2; font-weight: 700; box-shadow: var(--inner-shadow); }\n    .ols-course-cta-covalent h2 { margin: 0 0 14px; font-size: clamp(28px, 3.5vw, 42px); line-height: 1.15; font-weight: 800; letter-spacing: -0.03em; color: #111827; }\n    .ols-course-cta-intro { margin: 0 0 24px; color: var(--body-text); font-size: clamp(16px, 1.4vw, 18px); line-height: 1.7; font-weight: 300; }\n    .ols-course-cta-features { display: grid; grid-template-columns: repeat(2, minmax(0, 1fr)); gap: 14px; margin: 0 0 30px; }\n    .ols-course-feature { background: rgba(255, 255, 255, 0.78); border: 1px solid var(--border); border-radius: 18px; padding: 16px 18px; }\n    .ols-course-feature h3 { margin: 0 0 6px; color: var(--navy); font-size: 18px; line-height: 1.3; font-weight: 800; }\n    .ols-course-feature p { margin: 0; color: var(--body-text); font-size: 15px; line-height: 1.6; font-weight: 300; }\n    .ols-course-cta-bottom { display: flex; justify-content: center; padding-top: 22px; border-top: 1px solid var(--border); }\n    .ols-course-button { display: inline-flex; align-items: center; justify-content: center; padding: 15px 28px; border-radius: 999px; background: var(--navy); color: #ffffff; text-decoration: none; font-size: 16px; line-height: 1.2; font-weight: 800; box-shadow: 0 12px 26px rgba(28, 36, 75, 0.18); transition: transform 0.2s ease, background 0.2s ease, box-shadow 0.2s ease; }\n    .ols-course-button:hover { transform: translateY(-2px); background: var(--blue); color: #ffffff; box-shadow: 0 16px 32px rgba(37, 99, 235, 0.24); }\n    .ols-course-button-top { flex-shrink: 0; padding: 12px 22px; font-size: 15px; }\n\n    .ols-attribution-card {\n      background: linear-gradient(135deg, #ffffff, #f8fbff);\n      border: 1px solid rgba(28, 36, 75, 0.14);\n      border-radius: 28px;\n      box-shadow: 0 18px 45px rgba(28, 36, 75, 0.10);\n      padding: 34px;\n      margin-bottom: 24px;\n      overflow: hidden;\n      font-family: Poppins, Arial, sans-serif;\n      box-sizing: border-box;\n    }\n    .ols-attribution-card, .ols-attribution-card * { box-sizing: border-box; }\n    .ols-attribution-card p { margin: 0; font-size: 14px; line-height: 1.65; font-weight: 300; color: #667085; }\n    .ols-attribution-card strong { font-weight: 700; color: #1C244B; }\n\n    @media (max-width: 1050px) {\n      .ols-main { max-width: none; }\n      .ols-related-grid { grid-template-columns: repeat(2, minmax(0, 1fr)); }\n      .ols-course-cta-top { grid-template-columns: 1fr; }\n      .ols-course-cta-image-link { max-width: 520px; margin: 0 auto; }\n    }\n\n    @media (max-width: 760px) {\n      .ols-title-card, .ols-note-card, .ols-h5p-card, .ols-related-card, .ols-faq-card, .ols-attribution-card { padding: 24px 18px; border-radius: 22px; }\n      .ols-note-title { align-items: flex-start; }\n      .ols-related-grid, .ols-course-cta-features { grid-template-columns: 1fr; }\n      .ols-figure-card { border-radius: 22px; }\n      .ols-figure-image { min-height: 210px; padding: 14px; }\n      .ols-figure-caption { padding: 16px; }\n      .ols-table-wrap { border: none; background: transparent; }\n      .ols-table, .ols-table thead, .ols-table tbody, .ols-table th, .ols-table td, .ols-table tr { display: block; width: 100%; }\n      .ols-table { border-collapse: separate; border-spacing: 0; }\n      .ols-table thead { display: none; }\n      .ols-table tr { margin-bottom: 14px; border: 1px solid var(--border); border-radius: 18px; overflow: hidden; background: #ffffff; box-shadow: var(--inner-shadow); }\n      .ols-table td { border-bottom: 1px solid var(--border); padding: 14px 16px; overflow-wrap: anywhere; }\n      .ols-table td:last-child { border-bottom: none; }\n      .ols-table td::before { content: attr(data-label); 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.ols-figure-placeholder .ols-figure-caption p { margin: 10px 0 0; font-size: 14px; color: #667085; text-align: center; }\n\n    \/* inline checks (H5P re-flow, Sep 2026) *\/\n    .ols-h5p-card.ols-h5p-inline { padding: 26px 28px; border-left: 6px solid #7c3aed; }\n    .ols-h5p-card.ols-h5p-inline h2 { font-size: clamp(20px, 2.2vw, 27px); letter-spacing: -0.02em; }\n    .ols-h5p-card.ols-h5p-inline > p { margin: 8px 0 0; }\n    .ols-h5p-card.ols-h5p-inline .ols-h5p-frame { margin-top: 16px; padding: 14px; border-radius: 20px; }\n    .ols-h5p-kicker { display: inline-block; margin-bottom: 10px; padding: 5px 12px; border-radius: 999px; background: #ede9fe; color: #5b21b6; font-size: 12px; font-weight: 700; letter-spacing: 0.06em; text-transform: uppercase; }\n    .ols-h5p-card.ols-h5p-recap { border-left-color: #c9973a; background: linear-gradient(135deg, #ffffff 0%, #fff8e8 100%); }\n    .ols-h5p-recap .ols-h5p-kicker { background: #fdf0d2; color: #8a5a00; }\n    @media (max-width: 760px) { .ols-h5p-card.ols-h5p-inline { padding: 20px 16px; } }\n<\/style>\n\n  <aside class=\"ols-sidebar\">\n  <div class=\"ols-sidebar-header\">\n    <h3>Revision Notes<\/h3>\n    <p>A Level Chemistry<\/p>\n  <\/div>\n\n  <div class=\"ols-topic-group\">\n    <h4>3.1.9 Rate Equations<\/h4>\n\n    <ul class=\"ols-topic-list\">\n      <li>\n        <a href=\"https:\/\/www.onlinelearningsystem.net\/xyz\/revision-notes\/a-level-chemistry\/aqa\/3-1-9-rate-equations\/\">3.1.9 Rate Equations Overview<\/a>\n      <\/li>\n      <li>\n        <a href=\"https:\/\/www.onlinelearningsystem.net\/xyz\/revision-notes\/a-level-chemistry\/aqa\/3-1-9-rate-equations\/rate-equations-orders-and-the-rate-constant\/\">Rate Equations, Orders and the Rate Constant<\/a>\n      <\/li>\n      <li>\n        <a href=\"https:\/\/www.onlinelearningsystem.net\/xyz\/revision-notes\/a-level-chemistry\/aqa\/3-1-9-rate-equations\/techniques-for-measuring-rates\/\">Techniques for Measuring Rates<\/a>\n      <\/li>\n      <li>\n        <a href=\"https:\/\/www.onlinelearningsystem.net\/xyz\/revision-notes\/a-level-chemistry\/aqa\/3-1-9-rate-equations\/concentration-time-graphs-and-half-life\/\">Concentration\u2013Time Graphs and Half-Life<\/a>\n      <\/li>\n      <li>\n        <a href=\"https:\/\/www.onlinelearningsystem.net\/xyz\/revision-notes\/a-level-chemistry\/aqa\/3-1-9-rate-equations\/rate-concentration-graphs-and-the-initial-rates-method\/\">Rate\u2013Concentration Graphs and the Initial-Rates Method<\/a>\n      <\/li>\n      <li>\n        <a href=\"https:\/\/www.onlinelearningsystem.net\/xyz\/revision-notes\/a-level-chemistry\/aqa\/3-1-9-rate-equations\/the-iodine-propanone-reaction\/\">The Iodine\u2013Propanone Reaction<\/a>\n      <\/li>\n      <li>\n        <a href=\"https:\/\/www.onlinelearningsystem.net\/xyz\/revision-notes\/a-level-chemistry\/aqa\/3-1-9-rate-equations\/rate-determining-step-and-reaction-mechanisms\/\">Rate-Determining Step and Reaction Mechanisms<\/a>\n      <\/li>\n      <li>\n        <a href=\"https:\/\/www.onlinelearningsystem.net\/xyz\/revision-notes\/a-level-chemistry\/aqa\/3-1-9-rate-equations\/activation-energy-and-the-arrhenius-equation\/\">Activation Energy and the Arrhenius Equation<\/a>\n      <\/li>\n    <\/ul>\n  <\/div>\n\n  <div class=\"ols-topic-group\">\n    <h4>Other Sections<\/h4>\n\n    <ul class=\"ols-topic-list\">\n      <li>\n        <a href=\"https:\/\/www.onlinelearningsystem.net\/xyz\/revision-notes\/a-level-chemistry\/aqa\/3-1-5-kinetics\/\">3.1.5 Kinetics<\/a>\n      <\/li>\n      <li>\n        <a href=\"https:\/\/www.onlinelearningsystem.net\/xyz\/revision-notes\/a-level-chemistry\/aqa\/3-1-6-chemical-equilibria-le-chateliers-principle-and-kc\/\">3.1.6 Chemical Equilibria and Kc<\/a>\n      <\/li>\n      <li>\n        <a href=\"https:\/\/www.onlinelearningsystem.net\/xyz\/revision-notes\/a-level-chemistry\/aqa\/3-1-4-energetics\/\">3.1.4 Energetics<\/a>\n      <\/li>\n      <li>\n        <a href=\"https:\/\/www.onlinelearningsystem.net\/xyz\/revision-notes\/a-level-chemistry\/aqa\/required-practicals\/\">Required Practicals<\/a>\n      <\/li>\n    <\/ul>\n  <\/div>\n<\/aside>\n\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      item.classList.remove('active', 'active-main', 'parent-active');\r\n    });\r\n\r\n    sidebar.querySelectorAll('a[data-ols-disabled-parent=\"1\"], 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rate data are collected by sampling, quenching and titration or by colorimetry, why the reaction is zero order in iodine and first order in propanone and in hydrogen ions, and what that tells us about the rate-determining step and the mechanism.<\/p>\n\n        <div class=\"ols-badges\">\n<div class=\"ols-badge\">Paper 2 AQA<\/div>\n<div class=\"ols-badge\">3.1.9 Rate Equations<\/div>\n<div class=\"ols-badge\">7405\/2<\/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:<br><span>Dr. Mohammed Al-Fatah<\/span>\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        <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        View LinkedIn Profile\n      <\/a>\n\n    <\/div>\n\n  <\/div>\n      <\/header>\n\n      <article class=\"ols-note-card\">\n<div class=\"ols-note-title\">\n<div class=\"ols-note-icon\">1<\/div>\n<h2>The Reaction<\/h2>\n<\/div>\n<p>Propanone reacts with iodine in aqueous acid to give iodopropanone and hydrogen iodide: CH\u2083COCH\u2083 + I\u2082 \u2192 CH\u2083COCH\u2082I + HI.<\/p><p>The reaction is <strong>acid-catalysed<\/strong>: hydrogen ions do not appear in the overall equation but the reaction is far too slow without them.<\/p><p>It is the classic rate experiment for three reasons. Iodine is the only coloured substance, so its disappearance can be followed by eye, by titration or in a colorimeter. The other two concentrations can be set independently, so each order can be found in turn.<\/p><p>And the answer is surprising: the order with respect to iodine is zero, which forces the question of what the rate equation says about the mechanism.<\/p>\n<p>There is one complication. The product HI is a strong acid, so H\u207a is both the catalyst and a product: as the reaction runs, [H\u207a] rises and the reaction speeds itself up slightly, a mild <strong>autocatalysis<\/strong>.<\/p><p>It is controlled by using a large excess of acid, so that the H\u207a formed is negligible beside the H\u207a already there and [H\u207a] is effectively constant.<\/p>\n<div class=\"ols-key-box\">\n<p><strong>Key idea:<\/strong> Follow the one substance whose concentration is changing on its own: iodine, with propanone and acid in large excess.<\/p>\n<\/div>\n<div class=\"ols-zoom-card\">\n<div class=\"ols-zoom-card-image\">\n<a class=\"ols-lightbox-link\" href=\"https:\/\/www.onlinelearningsystem.net\/xyz\/wp-content\/uploads\/2026\/09\/t11x-propanonewhy.jpg\" aria-label=\"Open image full screen\">\n<img decoding=\"async\" class=\"ols-zoomable-img ols-lightbox-target\" src=\"https:\/\/www.onlinelearningsystem.net\/xyz\/wp-content\/uploads\/2026\/09\/t11x-propanonewhy.jpg\" alt=\"Poster of the propanone and iodine equation, three reasons it is used for rate studies, and the autocatalysis loop.\">\n<\/a>\n<\/div>\n<div class=\"ols-zoom-card-caption\"><p>Iodine is the only coloured species and the other concentrations can be set independently, while a large excess of acid stops the HI product from speeding the reaction up.<\/p><\/div>\n<\/div>\n<\/article>\n<article class=\"ols-note-card soft\">\n<div class=\"ols-note-title\">\n<div class=\"ols-note-icon\">2<\/div>\n<h2>Collecting the Data<\/h2>\n<\/div>\n<p><strong>Route A, sampling and titration.<\/strong> Known volumes of propanone and dilute sulfuric acid are mixed, the iodine solution is added and a clock started.<\/p><p>Every few minutes a sample is withdrawn with a pipette and run into a flask of <strong>sodium hydrogencarbonate<\/strong> solution. This <strong>quenches<\/strong> the reaction: the NaHCO\u2083 neutralises the H\u207a catalyst, so the reaction stops in the sample and the iodine present at that moment is fixed.<\/p><p>The iodine is then titrated with <strong>sodium thiosulfate<\/strong> solution, 2S\u2082O\u2083\u00b2\u207b + I\u2082 \u2192 S\u2084O\u2086\u00b2\u207b + 2I\u207b, adding a few drops of starch near the end point so that the blue-black colour vanishes sharply.<\/p><p>Each titre is proportional to [I\u2082] at the time the sample was quenched.<\/p>\n<p><strong>Route B, colorimetry.<\/strong> The mixture is placed in a colorimeter set to a filter that iodine absorbs (blue-green).<\/p><p>The absorbance falls as the brown colour fades, and a calibration curve of absorbance against known [I\u2082] converts each reading into a concentration.<\/p><p>Colorimetry gives many readings without disturbing the mixture and needs no quenching, but the solutions must be dilute enough for the absorbance to stay on the calibration curve.<\/p>\n<p>In both routes propanone and acid are in <strong>large excess<\/strong>, so their concentrations barely change and only [I\u2082] falls. The graph of [I\u2082] against time then shows the order with respect to iodine alone.<\/p><p>Repeating the experiment with different starting concentrations of propanone (acid fixed) and then of acid (propanone fixed) gives the initial rate in each case and so the other two orders.<\/p><p>In an initial-rates investigation such as Required practical 7 (rate by an initial-rate method and by continuous monitoring), the same choices (what to follow, how to stop the reaction, which reagents to put in excess) have to be made and justified.<\/p>\n<div class=\"ols-zoom-card\">\n<div class=\"ols-zoom-card-image\">\n<a class=\"ols-lightbox-link\" href=\"https:\/\/www.onlinelearningsystem.net\/xyz\/wp-content\/uploads\/2026\/09\/kinetics-t11-05-iodine-propanone.jpg\" aria-label=\"Open image full screen\">\n<img decoding=\"async\" class=\"ols-zoomable-img ols-lightbox-target\" src=\"https:\/\/www.onlinelearningsystem.net\/xyz\/wp-content\/uploads\/2026\/09\/kinetics-t11-05-iodine-propanone.jpg\" alt=\"Following the iodination of propanone by sampling and titration or by colorimetry, with graphs showing zero order in iodine and first order in propanone and H\u207a\">\n<\/a>\n<\/div>\n<div class=\"ols-zoom-card-caption\"><p>The two ways of following the iodine\u2013propanone reaction, and the three graphs that give the orders: zero in I\u2082, first in propanone and first in H\u207a.<\/p><\/div>\n<\/div>\n<div class=\"ols-key-box\">\n<p><strong>Exam wording:<\/strong> Quenching: &#8220;sodium hydrogencarbonate removes the H\u207a catalyst so the reaction stops and the iodine concentration at that time is fixed&#8221;. Excess: &#8220;so that the concentration of propanone (and of acid) is effectively constant and only [I\u2082] changes&#8221;.<\/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>Check: Collecting Rate Data by Sampling<\/h2>\n<p>Questions on the method: what a quench does, what the titration measures and why the other reactants are kept in excess, applied to reactions other than the one on this page.<\/p>\n<div class=\"ols-h5p-frame\"><div class=\"h5p-content\" data-content-id=\"1088\"><\/div><\/div>\n<\/section>\n<article class=\"ols-note-card\">\n<div class=\"ols-note-title\">\n<div class=\"ols-note-icon\">3<\/div>\n<h2>What the Results Show<\/h2>\n<\/div>\n<p>The graph of [I\u2082] against time is a <strong>straight line<\/strong> falling at a constant gradient. The rate does not change as iodine is used up, so the reaction is <strong>zero order with respect to iodine<\/strong>.<\/p><p>The same experiment run with double the propanone concentration gives a line of double the gradient: <strong>first order in propanone<\/strong>.<\/p><p>Doubling the acid concentration also doubles the gradient: <strong>first order in hydrogen ions<\/strong>. Put together:<\/p>\n<p style=\"text-align:center\"><strong>rate = k[CH\u2083COCH\u2083][H\u207a]<\/strong><\/p>\n<p>The overall order is 2, so k has the units mol\u207b\u00b9 dm\u00b3 s\u207b\u00b9 (rate in mol dm\u207b\u00b3 s\u207b\u00b9 divided by two concentrations).<\/p><p>Iodine is not in the rate equation at all, even though it is a reactant in the balanced equation.<\/p><div class=\"ols-key-box\"><p><strong>Key idea:<\/strong> this is the point the experiment exists to make: the orders come from the experiment and not from the stoichiometry.<\/p><\/div>\n<div class=\"ols-table-wrap\">\n<table class=\"ols-table\">\n<thead>\n<tr><th>Substance<\/th><th>How its order was found<\/th><th>Order<\/th><\/tr>\n<\/thead>\n<tbody>\n<tr><td><strong>I\u2082<\/strong><\/td><td>shape of the [I\u2082]\u2013time graph with the others in excess: straight line<\/td><td>0<\/td><\/tr>\n<tr><td><strong>CH\u2083COCH\u2083<\/strong><\/td><td>initial rate doubles when [propanone] doubles<\/td><td>1<\/td><\/tr>\n<tr><td><strong>H\u207a<\/strong><\/td><td>initial rate doubles when [H\u207a] doubles<\/td><td>1<\/td><\/tr>\n<\/tbody>\n<\/table>\n<\/div>\n<div class=\"ols-key-box\">\n<p><strong>Exam focus:<\/strong> State the evidence with the order: &#8220;the [I\u2082]\u2013time graph is a straight line, so the rate is constant as [I\u2082] falls, so zero order in iodine&#8221;.<\/p>\n<\/div>\n<\/article>\n<article class=\"ols-note-card soft\">\n<div class=\"ols-note-title\">\n<div class=\"ols-note-icon\">4<\/div>\n<h2>From Orders to Mechanism<\/h2>\n<\/div>\n<p>The rate equation contains only the species that take part in or before the <strong>rate-determining step<\/strong>, the slowest step of the mechanism.<\/p><p>Iodine is absent, so iodine can only react <strong>after<\/strong> the slow step.<\/p><p>Propanone and H\u207a are both present, each to the first power, so one molecule of propanone and one hydrogen ion are involved up to and including the slow step. Any proposed mechanism has to fit those facts.<\/p>\n<p>The accepted mechanism does. First the carbonyl oxygen of propanone is protonated by H\u207a (fast).<\/p><p>Then, in the slow step, a water molecule removes a hydrogen from a methyl group and the molecule rearranges to an <strong>enol<\/strong>, CH\u2082=C(OH)CH\u2083, releasing the H\u207a again.<\/p><p>Finally the electron-rich C=C of the enol attacks iodine (fast) and the carbonyl group re-forms, giving iodopropanone and HI.<\/p><p>The slow step involves the protonated propanone, formed from one propanone and one H\u207a, so the rate depends on [propanone][H\u207a]. Iodine reacts with the enol as fast as the enol appears, so its concentration does not matter.<\/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\/skel-t11-iodination-propanone-a.svg\" target=\"_blank\" rel=\"noopener\" aria-label=\"Open image fullscreen\">\n<img decoding=\"async\" src=\"https:\/\/www.onlinelearningsystem.net\/xyz\/wp-content\/uploads\/2026\/09\/skel-t11-iodination-propanone-a.svg\" alt=\"Mechanism of the acid-catalysed iodination of propanone, steps 1 and 2: protonation of the carbonyl oxygen, then slow loss of H\u207a from a methyl group to form the enol\" data-fullscreen-src=\"https:\/\/www.onlinelearningsystem.net\/xyz\/wp-content\/uploads\/2026\/09\/skel-t11-iodination-propanone-a.svg\" width=\"1448\" height=\"1452\">\n<\/a>\n<a class=\"ols-image-fullscreen-link\" href=\"https:\/\/www.onlinelearningsystem.net\/xyz\/wp-content\/uploads\/2026\/09\/skel-t11-iodination-propanone-b.svg\" target=\"_blank\" rel=\"noopener\" aria-label=\"Open image fullscreen\">\n<img decoding=\"async\" src=\"https:\/\/www.onlinelearningsystem.net\/xyz\/wp-content\/uploads\/2026\/09\/skel-t11-iodination-propanone-b.svg\" alt=\"Mechanism of the acid-catalysed iodination of propanone, step 3: the enol attacks iodine and loses H\u207a to give 1-iodopropanone, with the rate equation rate = k[CH\u2083COCH\u2083][H\u207a], zero order in iodine\" data-fullscreen-src=\"https:\/\/www.onlinelearningsystem.net\/xyz\/wp-content\/uploads\/2026\/09\/skel-t11-iodination-propanone-b.svg\" width=\"1628\" height=\"1492\">\n<\/a>\n<\/div>\n<div class=\"ols-figure-caption\"><p>The acid-catalysed iodination of propanone: fast protonation, slow enol formation (the rate-determining step) and fast attack of the enol on iodine.<\/p><\/div>\n<\/div>\n<p>Notice what the rate equation can and cannot do. It <strong>rules out<\/strong> any mechanism in which iodine reacts in or before the slow step, such as a single-step collision between propanone and I\u2082.<\/p><p>It <strong>does not prove<\/strong> the enol mechanism; other mechanisms with the same slow-step species would fit equally well.<\/p><p>The enol route is accepted because other evidence (bromination and deuterium exchange happen at the same rate) supports it.<\/p>\n<div class=\"ols-key-box\">\n<p><strong>Key idea:<\/strong> A rate equation identifies the species in the rate-determining step and rules out mechanisms that disagree with it. It cannot prove that a mechanism is right.<\/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>Check: Orders and the Rate-Determining Step<\/h2>\n<p>Interpret orders from rate data for other reactions: which species are in the rate-determining step, which react after it, and which proposed mechanisms are ruled out.<\/p>\n<div class=\"ols-h5p-frame\"><div class=\"h5p-content\" data-content-id=\"1089\"><\/div><\/div>\n<\/section>\n<article class=\"ols-note-card\">\n<div class=\"ols-note-title\">\n<div class=\"ols-note-icon\">5<\/div>\n<h2>Common Exam Points<\/h2>\n<\/div>\n<h3>Say<\/h3><p>&#8220;Zero order in iodine: the [I\u2082]\u2013time graph is a straight line, so the rate is independent of [I\u2082].&#8221; &#8220;Iodine does not appear in the rate equation, so it reacts after the rate-determining step.&#8221; &#8220;Propanone and acid are in large excess so their concentrations are effectively constant.&#8221;<\/p>\n<h3>Do not say<\/h3><p>&#8220;The order of iodine is 1 because one I\u2082 appears in the equation&#8221; (orders never come from the balanced equation). &#8220;The rate equation proves the mechanism.&#8221; &#8220;Sodium hydrogencarbonate removes the iodine&#8221; (it removes the acid).<\/p>\n<h3>Watch for<\/h3><p>A question that asks why the acid concentration is much larger than the iodine concentration: two reasons. One is to keep [H\u207a] constant so the order in propanone can be found; the other is to swamp the small amount of H\u207a produced as HI.<\/p><p>Also expect to be asked for the units of k for a second-order reaction: mol\u207b\u00b9 dm\u00b3 s\u207b\u00b9.<\/p>\n<\/article>\n<section class=\"ols-faq-card\">\n<h2>FAQs<\/h2>\n<p>Use these quick answers to check the iodine\u2013propanone reaction.<\/p>\n\n<div class=\"ols-faq-list\">\n<div class=\"ols-faq-item\">\n<h3>Why does the order with respect to iodine come out as zero?<\/h3>\n<p>Because iodine is not involved in the rate-determining step. The slow step is the acid-catalysed conversion of propanone to its enol; the enol then reacts with iodine in a fast step, so adding more iodine cannot speed things up.<\/p>\n<\/div>\n\n<div class=\"ols-faq-item\">\n<h3>How can I tell iodine is zero order just from the colorimeter trace?<\/h3>\n<p>The absorbance falls in a straight line, so the iodine concentration falls at a constant rate. A constant rate while the iodine is used up means the rate does not depend on [I\u2082].<\/p>\n<\/div>\n\n<div class=\"ols-faq-item\">\n<h3>Why is hydrogen ion in the rate equation when it is a catalyst?<\/h3>\n<p>Because it takes part in the rate-determining step, protonating the carbonyl oxygen before the enol forms. It is regenerated later, so it does not appear in the overall equation, but the rate still depends on how much of it is present.<\/p>\n<\/div>\n\n<div class=\"ols-faq-item\">\n<h3>What is used to quench the samples?<\/h3>\n<p>Sodium hydrogencarbonate solution. It neutralises the acid catalyst, and with no H\u207a the slow step effectively stops, so the iodine left in the sample can be titrated with sodium thiosulfate using starch as the indicator.<\/p>\n<\/div>\n\n<div class=\"ols-faq-item\">\n<h3>Why is the propanone concentration kept much larger than the iodine concentration?<\/h3>\n<p>So that only a small fraction of the propanone is used up while all the iodine reacts. Its concentration is then effectively constant, so any change in rate during a run is due to iodine alone, which is how the zero order is seen.<\/p>\n<\/div>\n<\/div>\n<\/section>\n<section class=\"ols-related-card\">\n<h2>Related 3.1.9 Rate Equations Pages<\/h2>\n<p>Use these pages to connect the ideas across 3.1.9 Rate Equations and the rest of the course.<\/p>\n<div class=\"ols-related-grid\">\n<a class=\"ols-related-item\" href=\"https:\/\/www.onlinelearningsystem.net\/xyz\/revision-notes\/a-level-chemistry\/aqa\/3-1-9-rate-equations\/rate-equations-orders-and-the-rate-constant\/\">Rate Equations, Orders and the Rate Constant<\/a>\n<a class=\"ols-related-item\" href=\"https:\/\/www.onlinelearningsystem.net\/xyz\/revision-notes\/a-level-chemistry\/aqa\/3-1-9-rate-equations\/techniques-for-measuring-rates\/\">Techniques for Measuring Rates<\/a>\n<a class=\"ols-related-item\" href=\"https:\/\/www.onlinelearningsystem.net\/xyz\/revision-notes\/a-level-chemistry\/aqa\/3-1-9-rate-equations\/concentration-time-graphs-and-half-life\/\">Concentration\u2013Time Graphs and Half-Life<\/a>\n<a class=\"ols-related-item\" href=\"https:\/\/www.onlinelearningsystem.net\/xyz\/revision-notes\/a-level-chemistry\/aqa\/3-1-9-rate-equations\/rate-concentration-graphs-and-the-initial-rates-method\/\">Rate\u2013Concentration Graphs and the Initial-Rates Method<\/a>\n<a class=\"ols-related-item\" href=\"https:\/\/www.onlinelearningsystem.net\/xyz\/revision-notes\/a-level-chemistry\/aqa\/3-1-9-rate-equations\/rate-determining-step-and-reaction-mechanisms\/\">Rate-Determining Step and Reaction Mechanisms<\/a>\n<a class=\"ols-related-item\" href=\"https:\/\/www.onlinelearningsystem.net\/xyz\/revision-notes\/a-level-chemistry\/aqa\/3-1-9-rate-equations\/activation-energy-and-the-arrhenius-equation\/\">Activation Energy and the Arrhenius Equation<\/a>\n<a class=\"ols-related-item\" href=\"https:\/\/www.onlinelearningsystem.net\/xyz\/revision-notes\/a-level-chemistry\/aqa\/3-1-9-rate-equations\/\">3.1.9 Rate Equations Overview<\/a>\n<\/div>\n<\/section>\n<section class=\"ols-attribution-card\">\n        <p><strong>Copyright and author footprint:<\/strong> This OLS revision page was written for Online Learning System by <strong>Dr. Mohammed Al-Fatah<\/strong>. It is designed for A Level Chemistry revision and should not be copied or redistributed without permission.<\/p>\n      <\/section>\n\n      <div class=\"ols-image-lightbox\" id=\"olsImageLightboxNatureCovalentBonding9ch0\" aria-hidden=\"true\" role=\"dialog\" aria-modal=\"true\" aria-label=\"Expanded revision image\">\n        <div class=\"ols-image-lightbox-inner\">\n          <button class=\"ols-image-lightbox-close\" type=\"button\" aria-label=\"Close enlarged image\">\u00d7<\/button>\n          <img decoding=\"async\" class=\"ols-image-lightbox-img\" src=\"\" alt=\"\">\n        <\/div>\n      <\/div>\n\n      <script>\n        (function(){\n          var page = document.querySelector(\".ols-nature-of-covalent-bonding-9ch0-page\");\n          if (!page) { return; }\n          var lightbox = page.querySelector(\"#olsImageLightboxNatureCovalentBonding9ch0\");\n          if (!lightbox) { return; }\n          var lightboxImage = lightbox.querySelector(\".ols-image-lightbox-img\");\n    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