{"id":224099,"date":"2025-06-02T17:34:09","date_gmt":"2025-06-02T17:34:09","guid":{"rendered":"https:\/\/learnexams.com\/blog\/?p=224099"},"modified":"2025-06-02T17:34:11","modified_gmt":"2025-06-02T17:34:11","slug":"select-the-correct-iupac-name-for-the-branched-chain-alkane","status":"publish","type":"post","link":"https:\/\/www.learnexams.com\/blog\/2025\/06\/02\/select-the-correct-iupac-name-for-the-branched-chain-alkane\/","title":{"rendered":"Select the correct IUPAC name for the branched chain alkane."},"content":{"rendered":"\n<p>Select the correct IUPAC name for the branched chain alkane. The name is: 3-propyl-5-ethyl-7-methyloctane 4-ethyl-6-ethyl-8-methylnonane 2-methyl-4,6-diethylnonane 4,6-diethyl-2-methylnonane<\/p>\n\n\n\n<figure class=\"wp-block-image size-full\"><img decoding=\"async\" src=\"https:\/\/learnexams.com\/blog\/wp-content\/uploads\/2025\/06\/image-35.png\" alt=\"\" class=\"wp-image-224100\"\/><\/figure>\n\n\n\n<p><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-ast-global-color-1-color\">The Correct Answer and Explanation is:<\/mark><\/strong><\/p>\n\n\n\n<h3 class=\"wp-block-heading\">Correct IUPAC Name:<\/h3>\n\n\n\n<p><strong>2-methyl-4,6-diethylnonane<\/strong><\/p>\n\n\n\n<hr class=\"wp-block-separator has-alpha-channel-opacity\"\/>\n\n\n\n<h3 class=\"wp-block-heading\">Explanation<\/h3>\n\n\n\n<p>To determine the correct IUPAC name of the given branched alkane, we need to follow the IUPAC rules for naming alkanes:<\/p>\n\n\n\n<h4 class=\"wp-block-heading\">1. <strong>Find the longest continuous carbon chain:<\/strong><\/h4>\n\n\n\n<p>From the image, the longest continuous carbon chain contains <strong>9 carbon atoms<\/strong>, so the parent hydrocarbon is <strong>nonane<\/strong>.<\/p>\n\n\n\n<h4 class=\"wp-block-heading\">2. <strong>Number the chain to give the lowest numbers to the substituents:<\/strong><\/h4>\n\n\n\n<p>We must number the chain from the end closest to the first branch. Starting from the left side gives substituent positions at <strong>2, 4, and 6<\/strong>, which are lower than numbering from the right.<\/p>\n\n\n\n<h4 class=\"wp-block-heading\">3. <strong>Identify the substituents:<\/strong><\/h4>\n\n\n\n<ul class=\"wp-block-list\">\n<li>At carbon <strong>2<\/strong>, there is a <strong>methyl group<\/strong> (\u2013CH\u2083).<\/li>\n\n\n\n<li>At carbon <strong>4<\/strong>, there is an <strong>ethyl group<\/strong> (\u2013CH\u2082CH\u2083).<\/li>\n\n\n\n<li>At carbon <strong>6<\/strong>, there is <strong>another ethyl group<\/strong>.<\/li>\n<\/ul>\n\n\n\n<p>This gives us:<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>One methyl group at position 2.<\/li>\n\n\n\n<li>Two ethyl groups at positions 4 and 6.<\/li>\n<\/ul>\n\n\n\n<h4 class=\"wp-block-heading\">4. <strong>Assemble the name:<\/strong><\/h4>\n\n\n\n<p>We use alphabetical order for substituents in the name:<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Ethyl comes before methyl.<\/li>\n\n\n\n<li>Two ethyl groups = <strong>diethyl<\/strong> \u2192 specify locations as <strong>4,6-diethyl<\/strong>.<\/li>\n\n\n\n<li>One methyl group at position 2 = <strong>2-methyl<\/strong>.<\/li>\n<\/ul>\n\n\n\n<p>Putting it all together:<br><strong>2-methyl-4,6-diethylnonane<\/strong><\/p>\n\n\n\n<h4 class=\"wp-block-heading\">5. <strong>Verify the options:<\/strong><\/h4>\n\n\n\n<ul class=\"wp-block-list\">\n<li><strong>Option A<\/strong>: Incorrect carbon count (octane = 8 C atoms).<\/li>\n\n\n\n<li><strong>Option B<\/strong>: Redundant \u201cethyl-ethyl\u201d listing, and numbering incorrect.<\/li>\n\n\n\n<li><strong>Option C<\/strong>: \u2705 Correct \u2013 matches our derived name.<\/li>\n\n\n\n<li><strong>Option D<\/strong>: Same name as C, but substituents not in proper alphabetical order.<\/li>\n<\/ul>\n\n\n\n<hr class=\"wp-block-separator has-alpha-channel-opacity\"\/>\n\n\n\n<h3 class=\"wp-block-heading\">\u2705 Final Answer: <strong>2-methyl-4,6-diethylnonane<\/strong><\/h3>\n\n\n\n<figure class=\"wp-block-image size-full\"><img decoding=\"async\" src=\"https:\/\/learnexams.com\/blog\/wp-content\/uploads\/2025\/06\/learnexams-banner9-20.jpeg\" alt=\"\" class=\"wp-image-224101\"\/><\/figure>\n","protected":false},"excerpt":{"rendered":"<p>Select the correct IUPAC name for the branched chain alkane. The name is: 3-propyl-5-ethyl-7-methyloctane 4-ethyl-6-ethyl-8-methylnonane 2-methyl-4,6-diethylnonane 4,6-diethyl-2-methylnonane The Correct Answer and Explanation is: Correct IUPAC Name: 2-methyl-4,6-diethylnonane Explanation To determine the correct IUPAC name of the given branched alkane, we need to follow the IUPAC rules for naming alkanes: 1. Find the longest continuous carbon [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"site-sidebar-layout":"default","site-content-layout":"","ast-site-content-layout":"default","site-content-style":"default","site-sidebar-style":"default","ast-global-header-display":"","ast-banner-title-visibility":"","ast-main-header-display":"","ast-hfb-above-header-display":"","ast-hfb-below-header-display":"","ast-hfb-mobile-header-display":"","site-post-title":"","ast-breadcrumbs-content":"","ast-featured-img":"","footer-sml-layout":"","ast-disable-related-posts":"","theme-transparent-header-meta":"","adv-header-id-meta":"","stick-header-meta":"","header-above-stick-meta":"","header-main-stick-meta":"","header-below-stick-meta":"","astra-migrate-meta-layouts":"default","ast-page-background-enabled":"default","ast-page-background-meta":{"desktop":{"background-color":"","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""},"tablet":{"background-color":"","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""},"mobile":{"background-color":"","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""}},"ast-content-background-meta":{"desktop":{"background-color":"var(--ast-global-color-5)","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""},"tablet":{"background-color":"var(--ast-global-color-5)","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""},"mobile":{"background-color":"var(--ast-global-color-5)","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""}},"footnotes":""},"categories":[25],"tags":[],"class_list":["post-224099","post","type-post","status-publish","format-standard","hentry","category-exams-certification"],"_links":{"self":[{"href":"https:\/\/www.learnexams.com\/blog\/wp-json\/wp\/v2\/posts\/224099","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.learnexams.com\/blog\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.learnexams.com\/blog\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.learnexams.com\/blog\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/www.learnexams.com\/blog\/wp-json\/wp\/v2\/comments?post=224099"}],"version-history":[{"count":0,"href":"https:\/\/www.learnexams.com\/blog\/wp-json\/wp\/v2\/posts\/224099\/revisions"}],"wp:attachment":[{"href":"https:\/\/www.learnexams.com\/blog\/wp-json\/wp\/v2\/media?parent=224099"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.learnexams.com\/blog\/wp-json\/wp\/v2\/categories?post=224099"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.learnexams.com\/blog\/wp-json\/wp\/v2\/tags?post=224099"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}