{"id":27349,"date":"2025-06-19T22:24:02","date_gmt":"2025-06-19T22:24:02","guid":{"rendered":"https:\/\/gaviki.com\/blog\/?p=27349"},"modified":"2025-06-19T22:24:07","modified_gmt":"2025-06-19T22:24:07","slug":"clear-all-ch3ch2cch2ch2ch3-lowest-boiling-point","status":"publish","type":"post","link":"https:\/\/gaviki.com\/blog\/clear-all-ch3ch2cch2ch2ch3-lowest-boiling-point\/","title":{"rendered":"Clear All CH3CH2CCH2CH2CH3 Lowest boiling point"},"content":{"rendered":"\n<p>Clear All CH3CH2CCH2CH2CH3 Lowest boiling point CH3CH2CH2CH2CH2CH2OH Intermediate boiling point Highest boiling point CH3CH2CH2CH2C-OH<\/p>\n\n\n\n<p><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-vivid-green-cyan-color\">The Correct Answer and Explanation is:<\/mark><\/strong><\/p>\n\n\n\n<p>To rank the compounds <strong>from lowest to highest boiling point<\/strong>, let\u2019s identify and analyze each structure:<\/p>\n\n\n\n<ol class=\"wp-block-list\">\n<li><strong>CH\u2083CH\u2082C\u2261CHCH\u2082CH\u2083<\/strong> \u2192 This is <strong>hex-2-yne<\/strong>, an <strong>alkyne<\/strong> with a linear structure.<\/li>\n\n\n\n<li><strong>CH\u2083CH\u2082CH\u2082CH\u2082CH\u2082CH\u2082OH<\/strong> \u2192 This is <strong>hexanol<\/strong>, a <strong>primary alcohol<\/strong>.<\/li>\n\n\n\n<li><strong>CH\u2083CH\u2082CH\u2082CH\u2082COOH<\/strong> \u2192 This is <strong>pentanoic acid<\/strong>, a <strong>carboxylic acid<\/strong>.<\/li>\n<\/ol>\n\n\n\n<hr class=\"wp-block-separator has-alpha-channel-opacity\"\/>\n\n\n\n<h3 class=\"wp-block-heading\">Correct Ranking by Boiling Point:<\/h3>\n\n\n\n<p><strong>Lowest boiling point: CH\u2083CH\u2082C\u2261CHCH\u2082CH\u2083 (hex-2-yne)<\/strong><br><strong>Intermediate boiling point: CH\u2083CH\u2082CH\u2082CH\u2082CH\u2082CH\u2082OH (hexanol)<\/strong><br><strong>Highest boiling point: CH\u2083CH\u2082CH\u2082CH\u2082COOH (pentanoic acid)<\/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>Boiling point depends on the <strong>strength of intermolecular forces<\/strong>. The stronger the forces, the higher the boiling point. The three main types of intermolecular forces are:<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li><strong>London dispersion forces<\/strong> (weakest)<\/li>\n\n\n\n<li><strong>Dipole-dipole interactions<\/strong><\/li>\n\n\n\n<li><strong>Hydrogen bonding<\/strong> (strongest of the three)<\/li>\n<\/ul>\n\n\n\n<p>Let\u2019s evaluate each compound:<\/p>\n\n\n\n<hr class=\"wp-block-separator has-alpha-channel-opacity\"\/>\n\n\n\n<ol class=\"wp-block-list\">\n<li><strong>CH\u2083CH\u2082C\u2261CHCH\u2082CH\u2083 (hex-2-yne)<\/strong>:<br>This compound has a <strong>triple bond<\/strong> and is nonpolar. The primary intermolecular force is <strong>London dispersion<\/strong>. It lacks groups like -OH or -COOH, so it cannot hydrogen bond. Therefore, it has the <strong>lowest boiling point<\/strong>.<\/li>\n<\/ol>\n\n\n\n<hr class=\"wp-block-separator has-alpha-channel-opacity\"\/>\n\n\n\n<ol start=\"2\" class=\"wp-block-list\">\n<li><strong>CH\u2083CH\u2082CH\u2082CH\u2082CH\u2082CH\u2082OH (hexanol)<\/strong>:<br>Hexanol has a <strong>hydroxyl group (-OH)<\/strong>, which allows for <strong>hydrogen bonding<\/strong>, increasing its boiling point. However, alcohols generally have lower boiling points than carboxylic acids because they form fewer hydrogen bonds per molecule.<\/li>\n<\/ol>\n\n\n\n<hr class=\"wp-block-separator has-alpha-channel-opacity\"\/>\n\n\n\n<ol start=\"3\" class=\"wp-block-list\">\n<li><strong>CH\u2083CH\u2082CH\u2082CH\u2082COOH (pentanoic acid)<\/strong>:<br>Carboxylic acids have both a <strong>hydroxyl and a carbonyl group<\/strong>, allowing them to form <strong>strong dimeric hydrogen bonds<\/strong>. This makes their boiling points <strong>higher than alcohols<\/strong> and far higher than hydrocarbons or alkynes.<\/li>\n<\/ol>\n\n\n\n<hr class=\"wp-block-separator has-alpha-channel-opacity\"\/>\n\n\n\n<h3 class=\"wp-block-heading\">Conclusion:<\/h3>\n\n\n\n<p>The correct order from <strong>lowest to highest boiling point<\/strong> is:<br><strong>CH\u2083CH\u2082C\u2261CHCH\u2082CH\u2083 &lt; CH\u2083CH\u2082CH\u2082CH\u2082CH\u2082CH\u2082OH &lt; CH\u2083CH\u2082CH\u2082CH\u2082COOH<\/strong>.<\/p>\n\n\n\n<figure class=\"wp-block-image size-full\"><img loading=\"lazy\" decoding=\"async\" width=\"852\" height=\"1024\" src=\"https:\/\/gaviki.com\/blog\/wp-content\/uploads\/2025\/06\/learnexams-banner8-156.jpeg\" alt=\"\" class=\"wp-image-27350\" srcset=\"https:\/\/gaviki.com\/blog\/wp-content\/uploads\/2025\/06\/learnexams-banner8-156.jpeg 852w, https:\/\/gaviki.com\/blog\/wp-content\/uploads\/2025\/06\/learnexams-banner8-156-250x300.jpeg 250w, https:\/\/gaviki.com\/blog\/wp-content\/uploads\/2025\/06\/learnexams-banner8-156-768x923.jpeg 768w\" sizes=\"auto, (max-width: 852px) 100vw, 852px\" \/><\/figure>\n","protected":false},"excerpt":{"rendered":"<p>Clear All CH3CH2CCH2CH2CH3 Lowest boiling point CH3CH2CH2CH2CH2CH2OH Intermediate boiling point Highest boiling point CH3CH2CH2CH2C-OH The Correct Answer and Explanation is: To rank the compounds from lowest to highest boiling point, let\u2019s identify and analyze each structure: Correct Ranking by Boiling Point: Lowest boiling point: CH\u2083CH\u2082C\u2261CHCH\u2082CH\u2083 (hex-2-yne)Intermediate boiling point: CH\u2083CH\u2082CH\u2082CH\u2082CH\u2082CH\u2082OH (hexanol)Highest boiling point: CH\u2083CH\u2082CH\u2082CH\u2082COOH (pentanoic acid) [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[1],"tags":[],"class_list":["post-27349","post","type-post","status-publish","format-standard","hentry","category-quiz-questions"],"_links":{"self":[{"href":"https:\/\/gaviki.com\/blog\/wp-json\/wp\/v2\/posts\/27349","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/gaviki.com\/blog\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/gaviki.com\/blog\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/gaviki.com\/blog\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/gaviki.com\/blog\/wp-json\/wp\/v2\/comments?post=27349"}],"version-history":[{"count":1,"href":"https:\/\/gaviki.com\/blog\/wp-json\/wp\/v2\/posts\/27349\/revisions"}],"predecessor-version":[{"id":27351,"href":"https:\/\/gaviki.com\/blog\/wp-json\/wp\/v2\/posts\/27349\/revisions\/27351"}],"wp:attachment":[{"href":"https:\/\/gaviki.com\/blog\/wp-json\/wp\/v2\/media?parent=27349"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/gaviki.com\/blog\/wp-json\/wp\/v2\/categories?post=27349"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/gaviki.com\/blog\/wp-json\/wp\/v2\/tags?post=27349"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}