{"id":2548,"date":"2026-04-14T08:58:28","date_gmt":"2026-04-14T07:58:28","guid":{"rendered":"https:\/\/www.onlinelearningsystem.net\/xyz\/?post_type=product&#038;p=2548"},"modified":"2026-06-24T07:31:03","modified_gmt":"2026-06-24T06:31:03","slug":"organic-chemistry-and-alkanes-topic-6ab","status":"publish","type":"product","link":"https:\/\/www.onlinelearningsystem.net\/xyz\/product\/organic-chemistry-and-alkanes-topic-6ab\/","title":{"rendered":"Organic Chemistry and Alkanes &#8211; Topic 6A\/6B"},"content":{"rendered":"<div class=\"ols-course-overview-topic-6ab\" style=\"max-width: 1100px; margin: 0 auto; font-family: Poppins, Arial, sans-serif; color: #1f2937; line-height: 1.7;\">\n<p><!-- INTRO BANNER --><\/p>\n<div style=\"background: linear-gradient(135deg, #f8fafc 0%, #eef2f7 100%); padding: 36px; border-radius: 20px; margin: 0 0 22px 0; border: 1px solid #e5e7eb; box-shadow: 0 10px 26px rgba(0,0,0,0.08);\">\n<h1 style=\"margin: 0 0 14px 0; font-size: 34px; font-weight: 600; line-height: 1.15; color: #1c244b; text-shadow: -9px 0 9px rgba(28,36,75,0.35);\">Organic Chemistry and Alkanes &#8211; Topic 6A\/B<\/h1>\n<div style=\"width: 88px; height: 5px; background: #c81e1e; border-radius: 999px; margin: 0 0 18px 0;\"><\/div>\n<p style=\"margin: 0; font-size: 19px; font-weight: 300; line-height: 1.8; color: #374151;\">The Organic Chemistry and Alkanes Topic 6A\/B Edexcel A Level Chemistry course provides approximately <strong>16 Hours of Guided Learning<\/strong>. Students work through guided video teaching, auto-marked MCQ practice, teacher-marked short-answer questions, and a specification assignment with a personalised progress report.<\/p>\n<\/div>\n<p><!-- STATS STRIP --><\/p>\n<div style=\"background: linear-gradient(135deg, #c81e1e 0%, #a91515 100%); padding: 18px; border-radius: 18px; margin: 0 0 34px 0; box-shadow: 0 10px 24px rgba(200,30,30,0.18);\">\n<div style=\"display: flex; flex-wrap: wrap; gap: 14px;\">\n<div style=\"flex: 1 1 200px; min-width: 180px; background: rgba(255,255,255,0.12); border: 1px solid rgba(255,255,255,0.18); border-radius: 14px; padding: 14px 16px; color: #ffffff;\">\n<div style=\"font-size: 12px; text-transform: uppercase; letter-spacing: 0.5px; opacity: 0.88;\">Guided Learning<\/div>\n<div style=\"font-size: 24px; font-weight: bold; line-height: 1.2;\">16 Hours<\/div>\n<\/div>\n<div style=\"flex: 1 1 200px; min-width: 180px; background: rgba(255,255,255,0.12); border: 1px solid rgba(255,255,255,0.18); border-radius: 14px; padding: 14px 16px; color: #ffffff;\">\n<div style=\"font-size: 12px; text-transform: uppercase; letter-spacing: 0.5px; opacity: 0.88;\">Video Lessons<\/div>\n<div style=\"font-size: 24px; font-weight: bold; line-height: 1.2;\">430 mins<\/div>\n<\/div>\n<div style=\"flex: 1 1 200px; min-width: 180px; background: rgba(255,255,255,0.12); border: 1px solid rgba(255,255,255,0.18); border-radius: 14px; padding: 14px 16px; color: #ffffff;\">\n<div style=\"font-size: 12px; text-transform: uppercase; letter-spacing: 0.5px; opacity: 0.88;\">MCQ Assessments<\/div>\n<div style=\"font-size: 24px; font-weight: bold; line-height: 1.2;\">73 Marks<\/div>\n<\/div>\n<div style=\"flex: 1 1 200px; min-width: 180px; background: rgba(255,255,255,0.12); border: 1px solid rgba(255,255,255,0.18); border-radius: 14px; padding: 14px 16px; color: #ffffff;\">\n<div style=\"font-size: 12px; text-transform: uppercase; letter-spacing: 0.5px; opacity: 0.88;\">SAQ Assessment<\/div>\n<div style=\"font-size: 24px; font-weight: bold; line-height: 1.2;\">30 Marks<\/div>\n<\/div>\n<\/div>\n<\/div>\n<p><!-- VIRTUAL LESSON --><\/p>\n<div style=\"background: #f3f4f6; padding: 30px; border-radius: 18px; margin: 0 0 28px 0; border: 1px solid #e5e7eb; box-shadow: 0 7px 18px rgba(0,0,0,0.08);\">\n<div style=\"display: inline-block; background: #ffffff; color: #c81e1e; border: 1px solid #f1d2d2; font-size: 12px; font-weight: bold; padding: 7px 13px; border-radius: 999px; margin: 0 0 14px 0;\">Guided Video Teaching<\/div>\n<h3 style=\"margin: 0 0 18px 0; font-size: 30px; font-weight: 600; line-height: 1.2; color: #1c244b; text-shadow: -9px 0 9px rgba(28,36,75,0.35); border-left: 6px solid #c81e1e; padding-left: 14px;\">Virtual Lesson<\/h3>\n<p style=\"margin: 0 0 16px 0; font-size: 19px; font-weight: 300; line-height: 1.8; color: #374151;\">The recorded lessons teach the key chemistry and the exam technique needed to apply it accurately.<\/p>\n<p style=\"margin: 0 0 22px 0; font-size: 18px; font-weight: 300; line-height: 1.8; color: #4b5563;\">Students pause during exam-practice sections, attempt questions independently, then review the worked explanations and mark scheme approach.<\/p>\n<div style=\"background: #ffffff; padding: 14px; border-radius: 14px; border: 1px solid #e5e7eb; box-shadow: 0 3px 10px rgba(0,0,0,0.05);\">\n<div style=\"position: relative; width: 100%; padding-bottom: 56.25%; height: 0; overflow: hidden; border-radius: 10px;\"><iframe style=\"position: absolute; top: 0; left: 0; width: 100%; height: 100%; border: 0; border-radius: 10px;\" title=\"Organic Chemistry and Alkanes Topic 6A\/B Edexcel A Level Chemistry Virtual Lesson\" src=\"https:\/\/www.youtube.com\/embed\/Fu_PA7Ec6Fk\" allowfullscreen=\"allowfullscreen\"><\/iframe><\/div>\n<\/div>\n<\/div>\n<p><!-- ASSIGNMENT REPORT --><\/p>\n<div style=\"background: #f3f4f6; padding: 30px; border-radius: 18px; margin: 0 0 34px 0; border: 1px solid #e5e7eb; box-shadow: 0 7px 18px rgba(0,0,0,0.08);\">\n<div style=\"display: inline-block; background: #ffffff; color: #c81e1e; border: 1px solid #f1d2d2; font-size: 12px; font-weight: bold; padding: 7px 13px; border-radius: 999px; margin: 0 0 14px 0;\">Specialist Marking<\/div>\n<h3 style=\"margin: 0 0 18px 0; font-size: 30px; font-weight: 600; line-height: 1.2; color: #1c244b; text-shadow: -9px 0 9px rgba(28,36,75,0.35); border-left: 6px solid #c81e1e; padding-left: 14px;\">Assignment &amp; Progress Report<\/h3>\n<p style=\"margin: 0 0 16px 0; font-size: 19px; font-weight: 300; line-height: 1.8; color: #374151;\">The 29-mark assignment assesses the full Topic 6A\/B specification, including organic formulae, IUPAC naming, structural isomerism, crude oil, fuels, alkanes, and radical substitution.<\/p>\n<p style=\"margin: 0 0 22px 0; font-size: 18px; font-weight: 300; line-height: 1.8; color: #4b5563;\">After marking, students receive a colour-coded progress report showing secure areas, partial understanding, and specification points requiring further revision.<\/p>\n<p><img decoding=\"async\" class=\"wp-image-2545 aligncenter\" style=\"display: block; width: 100%; max-width: 480px; height: auto; border-radius: 14px; margin: 0 auto; box-shadow: 0 6px 24px rgba(0,0,0,0.12);\" title=\"Organic Chemistry &amp; Alkanes Progress Report (Edexcel A Level)\" src=\"https:\/\/www.onlinelearningsystem.net\/xyz\/wp-content\/uploads\/2026\/04\/a-level-chemistry-organic-chemistry-alkanes-topic-6a-6b-progress-report.png\" alt=\"Organic chemistry and alkanes progress report showing student performance across Edexcel A Level specification requirements\" width=\"830\" height=\"1174\" \/><\/p>\n<\/div>\n<p><!-- MCQ --><\/p>\n<div style=\"background: #f3f4f6; padding: 30px; border-radius: 18px; margin: 0 0 28px 0; border: 1px solid #e5e7eb; box-shadow: 0 7px 18px rgba(0,0,0,0.08);\">\n<div style=\"display: inline-block; background: #ffffff; color: #c81e1e; border: 1px solid #f1d2d2; font-size: 12px; font-weight: bold; padding: 7px 13px; border-radius: 999px; margin: 0 0 14px 0;\">Instant Feedback<\/div>\n<h2 style=\"margin: 0 0 18px 0; font-size: 30px; font-weight: 600; line-height: 1.2; color: #1c244b; text-shadow: -9px 0 9px rgba(28,36,75,0.35); border-left: 6px solid #c81e1e; padding-left: 14px;\">Multiple Choice Question Assessments<\/h2>\n<p style=\"margin: 0 0 16px 0; font-size: 19px; font-weight: 300; line-height: 1.8; color: #374151;\">Four auto-marked MCQ quizzes provide 73 marks of targeted practice across Topic 6A\/B.<\/p>\n<p style=\"margin: 0 0 22px 0; font-size: 18px; font-weight: 300; line-height: 1.8; color: #4b5563;\">Each option includes diagnostic feedback, so students can see why the correct answer is right and why each incorrect option loses marks.<\/p>\n<div style=\"background: #ffffff; border: 1px solid #e5e7eb; border-radius: 14px; padding: 16px; margin: 0 0 22px 0;\">\n<div style=\"display: flex; flex-wrap: wrap; gap: 10px;\">\n<div style=\"flex: 1 1 130px; background: #fff7f7; border: 1px solid #f1d2d2; border-radius: 12px; padding: 12px; text-align: center;\">\n<div style=\"font-size: 12px; color: #6b7280; text-transform: uppercase; letter-spacing: 0.4px;\">MCQ A<\/div>\n<div style=\"font-size: 24px; font-weight: bold; color: #c81e1e; line-height: 1.2;\">20<\/div>\n<div style=\"font-size: 12px; color: #6b7280;\">marks available<\/div>\n<\/div>\n<div style=\"flex: 1 1 130px; background: #fff7f7; border: 1px solid #f1d2d2; border-radius: 12px; padding: 12px; text-align: center;\">\n<div style=\"font-size: 12px; color: #6b7280; text-transform: uppercase; letter-spacing: 0.4px;\">MCQ B<\/div>\n<div style=\"font-size: 24px; font-weight: bold; color: #c81e1e; line-height: 1.2;\">20<\/div>\n<div style=\"font-size: 12px; color: #6b7280;\">marks available<\/div>\n<\/div>\n<div style=\"flex: 1 1 130px; background: #fff7f7; border: 1px solid #f1d2d2; border-radius: 12px; padding: 12px; text-align: center;\">\n<div style=\"font-size: 12px; color: #6b7280; text-transform: uppercase; letter-spacing: 0.4px;\">MCQ C<\/div>\n<div style=\"font-size: 24px; font-weight: bold; color: #c81e1e; line-height: 1.2;\">20<\/div>\n<div style=\"font-size: 12px; color: #6b7280;\">marks available<\/div>\n<\/div>\n<div style=\"flex: 1 1 130px; background: #fff7f7; border: 1px solid #f1d2d2; border-radius: 12px; padding: 12px; text-align: center;\">\n<div style=\"font-size: 12px; color: #6b7280; text-transform: uppercase; letter-spacing: 0.4px;\">MCQ D<\/div>\n<div style=\"font-size: 24px; font-weight: bold; color: #c81e1e; line-height: 1.2;\">13<\/div>\n<div style=\"font-size: 12px; color: #6b7280;\">marks available<\/div>\n<\/div>\n<\/div>\n<\/div>\n<p><img decoding=\"async\" class=\"alignnone wp-image-2532\" style=\"display: block; width: 100%; max-width: 700px; height: auto; border-radius: 14px; margin: 0 auto; box-shadow: 0 6px 24px rgba(0,0,0,0.12);\" title=\"Cycloalkanes in Petrol - Octane Rating and Engine Knocking Explanation\" src=\"https:\/\/www.onlinelearningsystem.net\/xyz\/wp-content\/uploads\/2026\/04\/a-level-chemistry-alkene-chlorination-1-2-dichloro-4-methylpentane-mcq.webp\" alt=\"A Level Chemistry question on why cycloalkanes are added to petrol, showing incorrect student answer and feedback explaining octane rating and engine knocking.\" width=\"870\" height=\"779\" \/><\/p>\n<\/div>\n<p><!-- SAQ --><\/p>\n<div style=\"background: #f3f4f6; padding: 30px; border-radius: 18px; margin: 0 0 28px 0; border: 1px solid #e5e7eb; box-shadow: 0 7px 18px rgba(0,0,0,0.08);\">\n<div style=\"display: inline-block; background: #ffffff; color: #c81e1e; border: 1px solid #f1d2d2; font-size: 12px; font-weight: bold; padding: 7px 13px; border-radius: 999px; margin: 0 0 14px 0;\">Detailed Written Feedback<\/div>\n<h2 style=\"margin: 0 0 18px 0; font-size: 30px; font-weight: 600; line-height: 1.2; color: #1c244b; text-shadow: -9px 0 9px rgba(28,36,75,0.35); border-left: 6px solid #c81e1e; padding-left: 14px;\">Short Answer Question Assessment<\/h2>\n<p style=\"margin: 0 0 16px 0; font-size: 19px; font-weight: 300; line-height: 1.8; color: #374151;\">One teacher-marked short-answer quiz provides 30 marks of written exam practice across Topic 6A\/B.<\/p>\n<p style=\"margin: 0 0 16px 0; font-size: 18px; font-weight: 300; line-height: 1.8; color: #374151;\">Students submit written responses, structures, mechanisms, or uploaded working where required. Each submission is marked by a real chemistry teacher within three working days.<\/p>\n<p style=\"margin: 0 0 22px 0; font-size: 18px; font-weight: 300; line-height: 1.8; color: #4b5563;\">Feedback identifies what was correct, what was missing, and how to improve exam-standard written responses.<\/p>\n<div style=\"background: #ffffff; border: 1px solid #e5e7eb; border-radius: 14px; padding: 16px; margin: 0 0 22px 0;\">\n<div style=\"display: flex; flex-wrap: wrap; gap: 10px;\">\n<div style=\"flex: 1 1 160px; background: #fff7f7; border: 1px solid #f1d2d2; border-radius: 12px; padding: 12px; text-align: center;\">\n<div style=\"font-size: 12px; color: #6b7280; text-transform: uppercase; letter-spacing: 0.4px;\">SAQ A<\/div>\n<div style=\"font-size: 24px; font-weight: bold; color: #c81e1e; line-height: 1.2;\">30<\/div>\n<div style=\"font-size: 12px; color: #6b7280;\">marks available<\/div>\n<\/div>\n<\/div>\n<\/div>\n<p><img decoding=\"async\" class=\"alignnone wp-image-2533\" style=\"display: block; width: 100%; max-width: 700px; height: auto; border-radius: 14px; margin: 0 auto; box-shadow: 0 6px 24px rgba(0,0,0,0.12);\" title=\"a-level-chemistry-cycloalkanes-petrol-octane-rating-engine-knocking\" src=\"https:\/\/www.onlinelearningsystem.net\/xyz\/wp-content\/uploads\/2026\/04\/a-level-chemistry-cycloalkanes-petrol-octane-rating-engine-knocking.png\" alt=\"A Level Chemistry question on why cycloalkanes are added to petrol, showing incorrect student answer and feedback explaining octane rating and engine knocking.\" width=\"931\" height=\"840\" \/><\/p>\n<\/div>\n<p><!-- SPECIFICATION DESKTOP --><\/p>\n<div class=\"ols-spec-desktop-version\" style=\"background: #f3f4f6; padding: 30px; border-radius: 18px; margin: 0 0 28px 0; border: 1px solid #e5e7eb; box-shadow: 0 7px 18px rgba(0,0,0,0.08);\">\n<div style=\"display: inline-block; background: #ffffff; color: #c81e1e; border: 1px solid #f1d2d2; font-size: 12px; font-weight: bold; padding: 7px 13px; border-radius: 999px; margin: 0 0 14px 0;\">Exam Board Alignment<\/div>\n<h2 style=\"margin: 0 0 18px 0; font-size: 30px; font-weight: 600; line-height: 1.2; color: #1c244b; text-shadow: -9px 0 9px rgba(28,36,75,0.35); border-left: 6px solid #c81e1e; padding-left: 14px;\"><a style=\"color: #1c244b; text-decoration: none;\" href=\"https:\/\/qualifications.pearson.com\/content\/dam\/pdf\/A%20Level\/Chemistry\/2015\/Specification%20and%20sample%20assessments\/a-level-chemistry-2015-specification.pdf\" target=\"_blank\" rel=\"noopener\">Organic Chemistry and Alkanes Topic 6A\/B Edexcel A Level Chemistry<\/a><\/h2>\n<p style=\"margin: 0 0 18px 0; font-size: 19px; font-weight: 300; line-height: 1.8; color: #374151;\">This course covers the following Edexcel A Level Chemistry specification points:<\/p>\n<div style=\"display: flex; flex-direction: column; gap: 12px;\">\n<div style=\"display: flex; flex-wrap: nowrap; align-items: stretch; background: #ffffff; border: 1px solid #ead4d4; border-radius: 16px; overflow: hidden; box-shadow: 0 4px 12px rgba(0,0,0,0.05);\">\n<div style=\"flex: 0 0 90px; background: #c81e1e; color: #ffffff; font-size: 18px; font-weight: bold; display: flex; align-items: center; justify-content: center; padding: 18px 12px;\">6.1<\/div>\n<div style=\"flex: 1; padding: 16px 20px; font-size: 16px; font-weight: 300; line-height: 1.8; color: #374151;\">know that a hydrocarbon is a compound of hydrogen and carbon only<\/div>\n<\/div>\n<div style=\"display: flex; flex-wrap: nowrap; align-items: stretch; background: #ffffff; border: 1px solid #ead4d4; border-radius: 16px; overflow: hidden; box-shadow: 0 4px 12px rgba(0,0,0,0.05);\">\n<div style=\"flex: 0 0 90px; background: #c81e1e; color: #ffffff; font-size: 18px; font-weight: bold; display: flex; align-items: center; justify-content: center; padding: 18px 12px;\">6.2<\/div>\n<div style=\"flex: 1; padding: 16px 20px; font-size: 16px; font-weight: 300; line-height: 1.8; color: #374151;\">be able to represent organic molecules using empirical formulae, molecular formulae, general formulae, structural formulae, displayed formulae and skeletal formulae<\/div>\n<\/div>\n<div style=\"display: flex; flex-wrap: nowrap; align-items: stretch; background: #ffffff; border: 1px solid #ead4d4; border-radius: 16px; overflow: hidden; box-shadow: 0 4px 12px rgba(0,0,0,0.05);\">\n<div style=\"flex: 0 0 90px; background: #c81e1e; color: #ffffff; font-size: 18px; font-weight: bold; display: flex; align-items: center; justify-content: center; padding: 18px 12px;\">6.3<\/div>\n<div style=\"flex: 1; padding: 16px 20px; font-size: 16px; font-weight: 300; line-height: 1.8; color: #374151;\">know what is meant by the terms &#8216;homologous series&#8217; and &#8216;functional group&#8217;<\/div>\n<\/div>\n<div style=\"display: flex; flex-wrap: nowrap; align-items: stretch; background: #ffffff; border: 1px solid #ead4d4; border-radius: 16px; overflow: hidden; box-shadow: 0 4px 12px rgba(0,0,0,0.05);\">\n<div style=\"flex: 0 0 90px; background: #c81e1e; color: #ffffff; font-size: 18px; font-weight: bold; display: flex; align-items: center; justify-content: center; padding: 18px 12px;\">6.4<\/div>\n<div style=\"flex: 1; padding: 16px 20px; font-size: 16px; font-weight: 300; line-height: 1.8; color: #374151;\">be able to name compounds relevant to this specification using the rules of International Union of Pure and Applied Chemistry (IUPAC) nomenclature. Students will be expected to know prefixes for compounds up to C10<\/div>\n<\/div>\n<div style=\"display: flex; flex-wrap: nowrap; align-items: stretch; background: #ffffff; border: 1px solid #ead4d4; border-radius: 16px; overflow: hidden; box-shadow: 0 4px 12px rgba(0,0,0,0.05);\">\n<div style=\"flex: 0 0 90px; background: #c81e1e; color: #ffffff; font-size: 18px; font-weight: bold; display: flex; align-items: center; justify-content: center; padding: 18px 12px;\">6.5<\/div>\n<div style=\"flex: 1; padding: 16px 20px; font-size: 16px; font-weight: 300; line-height: 1.8; color: #374151;\">be able to classify reactions as addition, elimination, substitution, oxidation, reduction, hydrolysis or polymerisation<\/div>\n<\/div>\n<div style=\"display: flex; flex-wrap: nowrap; align-items: stretch; background: #ffffff; border: 1px solid #ead4d4; border-radius: 16px; overflow: hidden; box-shadow: 0 4px 12px rgba(0,0,0,0.05);\">\n<div style=\"flex: 0 0 90px; background: #c81e1e; color: #ffffff; font-size: 18px; font-weight: bold; display: flex; align-items: center; justify-content: center; padding: 18px 12px;\">6.6<\/div>\n<div style=\"flex: 1; padding: 16px 20px; font-size: 16px; font-weight: 300; line-height: 1.8; color: #374151;\">understand the term &#8216;structural isomerism&#8217; and be able to determine the possible structural, displayed and skeletal formulae of an organic molecule, given its molecular formula<\/div>\n<\/div>\n<div style=\"display: flex; flex-wrap: nowrap; align-items: stretch; background: #ffffff; border: 1px solid #ead4d4; border-radius: 16px; overflow: hidden; box-shadow: 0 4px 12px rgba(0,0,0,0.05);\">\n<div style=\"flex: 0 0 90px; background: #c81e1e; color: #ffffff; font-size: 18px; font-weight: bold; display: flex; align-items: center; justify-content: center; padding: 18px 12px;\">6.7<\/div>\n<div style=\"flex: 1; padding: 16px 20px; font-size: 16px; font-weight: 300; line-height: 1.8; color: #374151;\">understand the term &#8216;stereoisomerism&#8217;, as illustrated by E\/Z isomerism, including cis-trans isomerism where two of the substituent groups are the same<\/div>\n<\/div>\n<div style=\"display: flex; flex-wrap: nowrap; align-items: stretch; background: #ffffff; border: 1px solid #ead4d4; border-radius: 16px; overflow: hidden; box-shadow: 0 4px 12px rgba(0,0,0,0.05);\">\n<div style=\"flex: 0 0 90px; background: #c81e1e; color: #ffffff; font-size: 18px; font-weight: bold; display: flex; align-items: center; justify-content: center; padding: 18px 12px;\">6.8<\/div>\n<div style=\"flex: 1; padding: 16px 20px; font-size: 16px; font-weight: 300; line-height: 1.8; color: #374151;\">know the general formula for alkanes<\/div>\n<\/div>\n<div style=\"display: flex; flex-wrap: nowrap; align-items: stretch; background: #ffffff; border: 1px solid #ead4d4; border-radius: 16px; overflow: hidden; box-shadow: 0 4px 12px rgba(0,0,0,0.05);\">\n<div style=\"flex: 0 0 90px; background: #c81e1e; color: #ffffff; font-size: 18px; font-weight: bold; display: flex; align-items: center; justify-content: center; padding: 18px 12px;\">6.9<\/div>\n<div style=\"flex: 1; padding: 16px 20px; font-size: 16px; font-weight: 300; line-height: 1.8; color: #374151;\">know that alkanes and cycloalkanes are saturated hydrocarbons<\/div>\n<\/div>\n<div style=\"display: flex; flex-wrap: nowrap; align-items: stretch; background: #ffffff; border: 1px solid #ead4d4; border-radius: 16px; overflow: hidden; box-shadow: 0 4px 12px rgba(0,0,0,0.05);\">\n<div style=\"flex: 0 0 90px; background: #c81e1e; color: #ffffff; font-size: 18px; font-weight: bold; display: flex; align-items: center; justify-content: center; padding: 18px 12px;\">6.10<\/div>\n<div style=\"flex: 1; padding: 16px 20px; font-size: 16px; font-weight: 300; line-height: 1.8; color: #374151;\">understand that alkane fuels are obtained from the fractional distillation, cracking and reforming of crude oil<\/div>\n<\/div>\n<div style=\"display: flex; flex-wrap: nowrap; align-items: stretch; background: #ffffff; border: 1px solid #ead4d4; border-radius: 16px; overflow: hidden; box-shadow: 0 4px 12px rgba(0,0,0,0.05);\">\n<div style=\"flex: 0 0 90px; background: #c81e1e; color: #ffffff; font-size: 18px; font-weight: bold; display: flex; align-items: center; justify-content: center; padding: 18px 12px;\">6.11<\/div>\n<div style=\"flex: 1; padding: 16px 20px; font-size: 16px; font-weight: 300; line-height: 1.8; color: #374151;\">know that pollutants, including carbon monoxide, oxides of nitrogen and sulfur, carbon particulates and unburned hydrocarbons, are formed during the combustion of alkane fuels<\/div>\n<\/div>\n<div style=\"display: flex; flex-wrap: nowrap; align-items: stretch; background: #ffffff; border: 1px solid #ead4d4; border-radius: 16px; overflow: hidden; box-shadow: 0 4px 12px rgba(0,0,0,0.05);\">\n<div style=\"flex: 0 0 90px; background: #c81e1e; color: #ffffff; font-size: 18px; font-weight: bold; display: flex; align-items: center; justify-content: center; padding: 18px 12px;\">6.12<\/div>\n<div style=\"flex: 1; padding: 16px 20px; font-size: 16px; font-weight: 300; line-height: 1.8; color: #374151;\">understand the problems arising from pollutants from the combustion of fuels, limited to the toxicity of carbon monoxide and the acidity of oxides of nitrogen and sulfur<\/div>\n<\/div>\n<div style=\"display: flex; flex-wrap: nowrap; align-items: stretch; background: #ffffff; border: 1px solid #ead4d4; border-radius: 16px; overflow: hidden; box-shadow: 0 4px 12px rgba(0,0,0,0.05);\">\n<div style=\"flex: 0 0 90px; background: #c81e1e; color: #ffffff; font-size: 18px; font-weight: bold; display: flex; align-items: center; justify-content: center; padding: 18px 12px;\">6.13<\/div>\n<div style=\"flex: 1; padding: 16px 20px; font-size: 16px; font-weight: 300; line-height: 1.8; color: #374151;\">understand how the use of a catalytic converter solves some problems caused by pollutants<\/div>\n<\/div>\n<div style=\"display: flex; flex-wrap: nowrap; align-items: stretch; background: #ffffff; border: 1px solid #ead4d4; border-radius: 16px; overflow: hidden; box-shadow: 0 4px 12px rgba(0,0,0,0.05);\">\n<div style=\"flex: 0 0 90px; background: #c81e1e; color: #ffffff; font-size: 18px; font-weight: bold; display: flex; align-items: center; justify-content: center; padding: 18px 12px;\">6.14<\/div>\n<div style=\"flex: 1; padding: 16px 20px; font-size: 16px; font-weight: 300; line-height: 1.8; color: #374151;\">understand the use of alternative fuels, including biodiesel and alcohols derived from renewable sources such as plants, in terms of a comparison with non-renewable fossil fuels<\/div>\n<\/div>\n<div style=\"display: flex; flex-wrap: nowrap; align-items: stretch; background: #fff5f5; border: 1px solid #efcaca; border-radius: 16px; overflow: hidden; box-shadow: 0 4px 12px rgba(0,0,0,0.05);\">\n<div style=\"flex: 0 0 90px; background: #b91c1c; color: #ffffff; font-size: 18px; font-weight: bold; display: flex; align-items: center; justify-content: center; padding: 18px 12px;\">6.15<\/div>\n<div style=\"flex: 1; padding: 16px 20px;\">\n<div style=\"font-size: 16px; font-weight: 300; line-height: 1.8; color: #374151; margin: 0 0 12px 0;\">know that a radical:<\/div>\n<div style=\"display: flex; flex-direction: column; gap: 10px;\">\n<div style=\"display: flex; align-items: stretch; background: #ffffff; border: 1px solid #f1d5d5; border-radius: 12px; overflow: hidden;\">\n<div style=\"flex: 0 0 70px; background: #fca5a5; color: #7f1d1d; font-size: 14px; font-weight: bold; display: flex; align-items: center; justify-content: center; padding: 12px 10px;\">i<\/div>\n<div style=\"flex: 1; padding: 12px 16px; font-size: 15px; font-weight: 300; line-height: 1.8; color: #4b5563;\">is a species with an unpaired electron and is represented in mechanisms by a single dot<\/div>\n<\/div>\n<div style=\"display: flex; align-items: stretch; background: #ffffff; border: 1px solid #f1d5d5; border-radius: 12px; overflow: hidden;\">\n<div style=\"flex: 0 0 70px; background: #fca5a5; color: #7f1d1d; font-size: 14px; font-weight: bold; display: flex; align-items: center; justify-content: center; padding: 12px 10px;\">ii<\/div>\n<div style=\"flex: 1; padding: 12px 16px; font-size: 15px; font-weight: 300; line-height: 1.8; color: #4b5563;\">is formed by homolytic fission of a covalent bond and results in the formation of radicals<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<div style=\"display: flex; flex-wrap: nowrap; align-items: stretch; background: #fff5f5; border: 1px solid #efcaca; border-radius: 16px; overflow: hidden; box-shadow: 0 4px 12px rgba(0,0,0,0.05);\">\n<div style=\"flex: 0 0 90px; background: #b91c1c; color: #ffffff; font-size: 18px; font-weight: bold; display: flex; align-items: center; justify-content: center; padding: 18px 12px;\">6.16<\/div>\n<div style=\"flex: 1; padding: 16px 20px;\">\n<div style=\"font-size: 16px; font-weight: 300; line-height: 1.8; color: #374151; margin: 0 0 12px 0;\">understand the reactions of alkanes with:<\/div>\n<div style=\"display: flex; flex-direction: column; gap: 10px;\">\n<div style=\"display: flex; align-items: stretch; background: #ffffff; border: 1px solid #f1d5d5; border-radius: 12px; overflow: hidden;\">\n<div style=\"flex: 0 0 70px; background: #fca5a5; color: #7f1d1d; font-size: 14px; font-weight: bold; display: flex; align-items: center; justify-content: center; padding: 12px 10px;\">i<\/div>\n<div style=\"flex: 1; padding: 12px 16px; font-size: 15px; font-weight: 300; line-height: 1.8; color: #4b5563;\">oxygen in the air (combustion)<\/div>\n<\/div>\n<div style=\"display: flex; align-items: stretch; background: #ffffff; border: 1px solid #f1d5d5; border-radius: 12px; overflow: hidden;\">\n<div style=\"flex: 0 0 70px; background: #fca5a5; color: #7f1d1d; font-size: 14px; font-weight: bold; display: flex; align-items: center; justify-content: center; padding: 12px 10px;\">ii<\/div>\n<div style=\"flex: 1; padding: 12px 16px; font-size: 15px; font-weight: 300; line-height: 1.8; color: #4b5563;\">halogens, in terms of the mechanism of radical substitution through initiation, propagation and termination steps<\/div>\n<\/div>\n<div style=\"display: flex; align-items: stretch; background: #ffffff; border: 1px solid #f1d5d5; border-radius: 12px; overflow: hidden;\">\n<div style=\"flex: 0 0 70px; background: #fca5a5; color: #7f1d1d; font-size: 14px; font-weight: bold; display: flex; align-items: center; justify-content: center; padding: 12px 10px;\">iii<\/div>\n<div style=\"flex: 1; padding: 12px 16px; font-size: 15px; font-weight: 300; line-height: 1.8; color: #4b5563;\">The use of curly half-arrows is not expected in this mechanism<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<div style=\"display: flex; flex-wrap: nowrap; align-items: stretch; background: #ffffff; border: 1px solid #ead4d4; border-radius: 16px; overflow: hidden; box-shadow: 0 4px 12px rgba(0,0,0,0.05);\">\n<div style=\"flex: 0 0 90px; background: #c81e1e; color: #ffffff; font-size: 18px; font-weight: bold; display: flex; align-items: center; justify-content: center; padding: 18px 12px;\">6.17<\/div>\n<div style=\"flex: 1; padding: 16px 20px; font-size: 16px; font-weight: 300; line-height: 1.8; color: #374151;\">understand the limitations of the use of radical substitution reactions in the synthesis of organic molecules, in terms of further substitution reactions and the formation of a mixture of products<\/div>\n<\/div>\n<\/div>\n<\/div>\n<p><!-- SPECIFICATION MOBILE --><\/p>\n<div class=\"ols-spec-mobile-version\" style=\"max-width: 1100px; margin: 0 auto 28px auto; font-family: Arial, Helvetica, sans-serif; color: #1f2937; line-height: 1.7;\">\n<div style=\"background: linear-gradient(135deg, #fff7f7 0%, #fef2f2 100%); border: 1px solid #f3d6d6; border-radius: 22px; padding: 26px; box-shadow: 0 10px 26px rgba(0,0,0,0.08);\">\n<div style=\"margin: 0 0 22px 0;\">\n<div style=\"display: inline-block; background: #ffffff; color: #c81e1e; border: 1px solid #f1d2d2; font-size: 12px; font-weight: bold; padding: 7px 13px; border-radius: 999px; margin: 0 0 14px 0;\">Specification Coverage<\/div>\n<h2 style=\"margin: 0 0 12px 0; font-size: 34px; line-height: 1.2; color: #111827;\">Students will be assessed on their ability to:<\/h2>\n<div style=\"width: 88px; height: 5px; background: #c81e1e; border-radius: 999px; margin: 0 0 16px 0;\"><\/div>\n<p style=\"margin: 0; font-size: 18px; line-height: 1.8; color: #374151;\">The following specification points outline the knowledge and skills students are expected to demonstrate.<\/p>\n<\/div>\n<div style=\"display: flex; flex-direction: column; gap: 12px;\">\n<div style=\"background: #ffffff; border: 1px solid #ead4d4; border-radius: 16px; overflow: hidden; box-shadow: 0 4px 12px rgba(0,0,0,0.05);\">\n<div style=\"background: #c81e1e; color: #ffffff; font-size: 16px; font-weight: bold; text-align: center; height: 34px; line-height: 34px;\">6.1<\/div>\n<div style=\"padding: 18px 20px; font-size: 17px; line-height: 1.8; color: #374151;\">know that a hydrocarbon is a compound of hydrogen and carbon only<\/div>\n<\/div>\n<div style=\"background: #ffffff; border: 1px solid #ead4d4; border-radius: 16px; overflow: hidden; box-shadow: 0 4px 12px rgba(0,0,0,0.05);\">\n<div style=\"background: #c81e1e; color: #ffffff; font-size: 16px; font-weight: bold; text-align: center; height: 34px; line-height: 34px;\">6.2<\/div>\n<div style=\"padding: 18px 20px; font-size: 17px; line-height: 1.8; color: #374151;\">be able to represent organic molecules using empirical formulae, molecular formulae, general formulae, structural formulae, displayed formulae and skeletal formulae<\/div>\n<\/div>\n<div style=\"background: #ffffff; border: 1px solid #ead4d4; border-radius: 16px; overflow: hidden; box-shadow: 0 4px 12px rgba(0,0,0,0.05);\">\n<div style=\"background: #c81e1e; color: #ffffff; font-size: 16px; font-weight: bold; text-align: center; height: 34px; line-height: 34px;\">6.3<\/div>\n<div style=\"padding: 18px 20px; font-size: 17px; line-height: 1.8; color: #374151;\">know what is meant by the terms \u2018homologous series\u2019 and \u2018functional group\u2019<\/div>\n<\/div>\n<div style=\"background: #ffffff; border: 1px solid #ead4d4; border-radius: 16px; overflow: hidden; box-shadow: 0 4px 12px rgba(0,0,0,0.05);\">\n<div style=\"background: #c81e1e; color: #ffffff; font-size: 16px; font-weight: bold; text-align: center; height: 34px; line-height: 34px;\">6.4<\/div>\n<div style=\"padding: 18px 20px; font-size: 17px; line-height: 1.8; color: #374151;\">be able to name compounds relevant to this specification using the rules of International Union of Pure and Applied Chemistry (IUPAC) nomenclature Students will be expected to know prefixes for compounds up to C10<\/div>\n<\/div>\n<div style=\"background: #ffffff; border: 1px solid #ead4d4; border-radius: 16px; overflow: hidden; box-shadow: 0 4px 12px rgba(0,0,0,0.05);\">\n<div style=\"background: #c81e1e; color: #ffffff; font-size: 16px; font-weight: bold; text-align: center; height: 34px; line-height: 34px;\">6.5<\/div>\n<div style=\"padding: 18px 20px; font-size: 17px; line-height: 1.8; color: #374151;\">be able to classify reactions as addition, elimination, substitution, oxidation, reduction, hydrolysis or polymerisation<\/div>\n<\/div>\n<div style=\"background: #ffffff; border: 1px solid #ead4d4; border-radius: 16px; overflow: hidden; box-shadow: 0 4px 12px rgba(0,0,0,0.05);\">\n<div style=\"background: #c81e1e; color: #ffffff; font-size: 16px; font-weight: bold; text-align: center; height: 34px; line-height: 34px;\">6.6<\/div>\n<div style=\"padding: 18px 20px; font-size: 17px; line-height: 1.8; color: #374151;\">understand the term \u2018structural isomerism\u2019 and determine the possible structural, displayed and skeletal formulae of an organic molecule, given its molecular formula<\/div>\n<\/div>\n<div style=\"background: #ffffff; border: 1px solid #ead4d4; border-radius: 16px; overflow: hidden; box-shadow: 0 4px 12px rgba(0,0,0,0.05);\">\n<div style=\"background: #c81e1e; color: #ffffff; font-size: 16px; font-weight: bold; text-align: center; height: 34px; line-height: 34px;\">6.7<\/div>\n<div style=\"padding: 18px 20px; font-size: 17px; line-height: 1.8; color: #374151;\">understand the term \u2018stereoisomerism\u2019, as illustrated by E\/Z isomerism, including cis-trans isomerism where two of the substituent groups are the same<\/div>\n<\/div>\n<div style=\"background: #ffffff; border: 1px solid #ead4d4; border-radius: 16px; overflow: hidden; box-shadow: 0 4px 12px rgba(0,0,0,0.05);\">\n<div style=\"background: #c81e1e; color: #ffffff; font-size: 16px; font-weight: bold; text-align: center; height: 34px; line-height: 34px;\">6.8<\/div>\n<div style=\"padding: 18px 20px; font-size: 17px; line-height: 1.8; color: #374151;\">know the general formula for alkanes<\/div>\n<\/div>\n<div style=\"background: #ffffff; border: 1px solid #ead4d4; border-radius: 16px; overflow: hidden; box-shadow: 0 4px 12px rgba(0,0,0,0.05);\">\n<div style=\"background: #c81e1e; color: #ffffff; font-size: 16px; font-weight: bold; text-align: center; height: 34px; line-height: 34px;\">6.9<\/div>\n<div style=\"padding: 18px 20px; font-size: 17px; line-height: 1.8; color: #374151;\">know that alkanes and cycloalkanes are saturated hydrocarbons<\/div>\n<\/div>\n<div style=\"background: #ffffff; border: 1px solid #ead4d4; border-radius: 16px; overflow: hidden; box-shadow: 0 4px 12px rgba(0,0,0,0.05);\">\n<div style=\"background: #c81e1e; color: #ffffff; font-size: 16px; font-weight: bold; text-align: center; height: 34px; line-height: 34px;\">6.10<\/div>\n<div style=\"padding: 18px 20px; font-size: 17px; line-height: 1.8; color: #374151;\">understand that alkane fuels are obtained from the fractional distillation, cracking and reforming of crude oil. Reforming is described as the processing of straight-chain hydrocarbons into branched-chain alkanes and cyclic hydrocarbons for efficient combustion.<\/div>\n<\/div>\n<div style=\"background: #ffffff; border: 1px solid #ead4d4; border-radius: 16px; overflow: hidden; box-shadow: 0 4px 12px rgba(0,0,0,0.05);\">\n<div style=\"background: #c81e1e; color: #ffffff; font-size: 16px; font-weight: bold; text-align: center; height: 34px; line-height: 34px;\">6.11<\/div>\n<div style=\"padding: 18px 20px; font-size: 17px; line-height: 1.8; color: #374151;\">know that pollutants, including carbon monoxide, oxides of nitrogen and sulfur, carbon particulates and unburned hydrocarbons, are formed during the combustion of alkane fuels<\/div>\n<\/div>\n<div style=\"background: #ffffff; border: 1px solid #ead4d4; border-radius: 16px; overflow: hidden; box-shadow: 0 4px 12px rgba(0,0,0,0.05);\">\n<div style=\"background: #c81e1e; color: #ffffff; font-size: 16px; font-weight: bold; text-align: center; height: 34px; line-height: 34px;\">6.12<\/div>\n<div style=\"padding: 18px 20px; font-size: 17px; line-height: 1.8; color: #374151;\">understand the problems arising from pollutants from the combustion of fuels, limited to the toxicity of carbon monoxide and the acidity of oxides of nitrogen and sulfur<\/div>\n<\/div>\n<div style=\"background: #ffffff; border: 1px solid #ead4d4; border-radius: 16px; overflow: hidden; box-shadow: 0 4px 12px rgba(0,0,0,0.05);\">\n<div style=\"background: #c81e1e; color: #ffffff; font-size: 16px; font-weight: bold; text-align: center; height: 34px; line-height: 34px;\">6.13<\/div>\n<div style=\"padding: 18px 20px; font-size: 17px; line-height: 1.8; color: #374151;\">understand how the use of a catalytic converter solves some problems caused by pollutants<\/div>\n<\/div>\n<div style=\"background: #ffffff; border: 1px solid #ead4d4; border-radius: 16px; overflow: hidden; box-shadow: 0 4px 12px rgba(0,0,0,0.05);\">\n<div style=\"background: #c81e1e; color: #ffffff; font-size: 16px; font-weight: bold; text-align: center; height: 34px; line-height: 34px;\">6.14<\/div>\n<div style=\"padding: 18px 20px; font-size: 17px; line-height: 1.8; color: #374151;\">understand the use of alternative fuels, including biodiesel and alcohols derived from renewable sources such as plants, in terms of a comparison with non-renewable fossil fuels<\/div>\n<\/div>\n<div style=\"background: #fff5f5; border: 1px solid #efcaca; border-radius: 16px; overflow: hidden; box-shadow: 0 4px 12px rgba(0,0,0,0.05);\">\n<div style=\"background: #b91c1c; color: #ffffff; font-size: 16px; font-weight: bold; text-align: center; height: 34px; line-height: 34px;\">6.15<\/div>\n<div style=\"padding: 18px 20px;\">\n<div style=\"font-size: 17px; line-height: 1.8; color: #374151; margin: 0 0 12px 0;\">know that a radical:<\/div>\n<div style=\"display: flex; flex-direction: column; gap: 10px;\">\n<div style=\"background: #ffffff; border: 1px solid #f1d5d5; border-radius: 12px; overflow: hidden;\">\n<div style=\"background: #fca5a5; color: #7f1d1d; font-size: 14px; font-weight: bold; text-align: center; height: 30px; line-height: 30px;\">i<\/div>\n<div style=\"padding: 14px 16px; font-size: 16px; line-height: 1.8; color: #4b5563;\">is a species with an unpaired electron and is represented in mechanisms by a single dot<\/div>\n<\/div>\n<div style=\"background: #ffffff; border: 1px solid #f1d5d5; border-radius: 12px; overflow: hidden;\">\n<div style=\"background: #fca5a5; color: #7f1d1d; font-size: 14px; font-weight: bold; text-align: center; height: 30px; line-height: 30px;\">ii<\/div>\n<div style=\"padding: 14px 16px; font-size: 16px; line-height: 1.8; color: #4b5563;\">is formed by homolytic fission of a covalent bond and results in the formation of radicals<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<div style=\"background: #fff5f5; border: 1px solid #efcaca; border-radius: 16px; overflow: hidden; box-shadow: 0 4px 12px rgba(0,0,0,0.05);\">\n<div style=\"background: #b91c1c; color: #ffffff; font-size: 16px; font-weight: bold; text-align: center; height: 34px; line-height: 34px;\">6.16<\/div>\n<div style=\"padding: 18px 20px;\">\n<div style=\"font-size: 17px; line-height: 1.8; color: #374151; margin: 0 0 12px 0;\">understand the reactions of alkanes with:<\/div>\n<div style=\"display: flex; flex-direction: column; gap: 10px;\">\n<div style=\"background: #ffffff; border: 1px solid #f1d5d5; border-radius: 12px; overflow: hidden;\">\n<div style=\"background: #fca5a5; color: #7f1d1d; font-size: 14px; font-weight: bold; text-align: center; height: 30px; line-height: 30px;\">i<\/div>\n<div style=\"padding: 14px 16px; font-size: 16px; line-height: 1.8; color: #4b5563;\">oxygen in air (combustion)<\/div>\n<\/div>\n<div style=\"background: #ffffff; border: 1px solid #f1d5d5; border-radius: 12px; overflow: hidden;\">\n<div style=\"background: #fca5a5; color: #7f1d1d; font-size: 14px; font-weight: bold; text-align: center; height: 30px; line-height: 30px;\">ii<\/div>\n<div style=\"padding: 14px 16px; font-size: 16px; line-height: 1.8; color: #4b5563;\">halogens, in terms of the mechanism of radical substitution through initiation, propagation and termination steps. The use of curly half-arrows is not expected in this mechanism.<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<div style=\"background: #ffffff; border: 1px solid #ead4d4; border-radius: 16px; overflow: hidden; box-shadow: 0 4px 12px rgba(0,0,0,0.05);\">\n<div style=\"background: #c81e1e; color: #ffffff; font-size: 16px; font-weight: bold; text-align: center; height: 34px; line-height: 34px;\">6.17<\/div>\n<div style=\"padding: 18px 20px; font-size: 17px; line-height: 1.8; color: #374151;\">understand the limitations of the use of radical substitution reactions in the synthesis of organic molecules, in terms of further substitution reactions and the formation of a mixture of products<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<p><!-- CTA --><\/p>\n<div style=\"background: linear-gradient(135deg, #c81e1e 0%, #a91515 100%); padding: 30px; border-radius: 20px; margin: 0 0 12px 0; color: #ffffff; box-shadow: 0 10px 26px rgba(200,30,30,0.22);\">\n<div style=\"font-size: 12px; font-weight: bold; letter-spacing: 0.5px; text-transform: uppercase; opacity: 0.9; margin: 0 0 10px 0;\">Complete Topic Package<\/div>\n<h3 style=\"margin: 0 0 12px 0; font-size: 30px; font-weight: 600; line-height: 1.2; color: #ffffff; text-shadow: -9px 0 9px rgba(28,36,75,0.35);\">Learn the content, practise exam questions, and identify exactly where marks are being lost.<\/h3>\n<p style=\"margin: 0 0 18px 0; font-size: 18px; font-weight: 300; line-height: 1.8; color: #fef2f2;\">This course combines guided video teaching, diagnostic MCQs, teacher-marked written assessment, and detailed specification reporting for Edexcel A Level Chemistry.<\/p>\n<div style=\"display: inline-block; background: #ffffff; color: #c81e1e; font-weight: bold; font-size: 15px; padding: 12px 18px; border-radius: 999px;\">Exam-focused learning with clear performance feedback<\/div>\n<\/div>\n<\/div>\n","protected":false},"excerpt":{"rendered":"<p>Organic Chemistry and Alkanes &#8211; Topic 6A\/B The Organic Chemistry and Alkanes Topic 6A\/B Edexcel A Level Chemistry course provides approximately 16 Hours of Guided Learning. Students work through guided video teaching, auto-marked MCQ practice, teacher-marked short-answer questions, and a specification assignment with a personalised progress report. Guided Learning 16 Hours Video Lessons 430 mins [&hellip;]<\/p>\n","protected":false},"featured_media":2934,"comment_status":"closed","ping_status":"closed","template":"","meta":[],"product_brand":[],"product_cat":[329],"product_tag":[],"class_list":["post-2548","product","type-product","status-publish","has-post-thumbnail","product_cat-edexcel-a-level-chemistry","first","outofstock","virtual","purchasable","product-type-simple"],"_links":{"self":[{"href":"https:\/\/www.onlinelearningsystem.net\/xyz\/wp-json\/wp\/v2\/product\/2548","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.onlinelearningsystem.net\/xyz\/wp-json\/wp\/v2\/product"}],"about":[{"href":"https:\/\/www.onlinelearningsystem.net\/xyz\/wp-json\/wp\/v2\/types\/product"}],"replies":[{"embeddable":true,"href":"https:\/\/www.onlinelearningsystem.net\/xyz\/wp-json\/wp\/v2\/comments?post=2548"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/www.onlinelearningsystem.net\/xyz\/wp-json\/wp\/v2\/media\/2934"}],"wp:attachment":[{"href":"https:\/\/www.onlinelearningsystem.net\/xyz\/wp-json\/wp\/v2\/media?parent=2548"}],"wp:term":[{"taxonomy":"product_brand","embeddable":true,"href":"https:\/\/www.onlinelearningsystem.net\/xyz\/wp-json\/wp\/v2\/product_brand?post=2548"},{"taxonomy":"product_cat","embeddable":true,"href":"https:\/\/www.onlinelearningsystem.net\/xyz\/wp-json\/wp\/v2\/product_cat?post=2548"},{"taxonomy":"product_tag","embeddable":true,"href":"https:\/\/www.onlinelearningsystem.net\/xyz\/wp-json\/wp\/v2\/product_tag?post=2548"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}