{"id":27353,"date":"2025-06-19T22:27:09","date_gmt":"2025-06-19T22:27:09","guid":{"rendered":"https:\/\/gaviki.com\/blog\/?p=27353"},"modified":"2025-06-19T22:27:10","modified_gmt":"2025-06-19T22:27:10","slug":"which-compound-will-have-the-highest-boiling-point","status":"publish","type":"post","link":"https:\/\/gaviki.com\/blog\/which-compound-will-have-the-highest-boiling-point\/","title":{"rendered":"Which compound will have the highest boiling point"},"content":{"rendered":"\n<p>Which compound will have the highest boiling point? CH3CH2CH2CH2OH CH3CH2CH2CH2Cl CH3CH2CH=CHCH3 CH3CH2CH2CH2OCH2CH3<\/p>\n\n\n\n<figure class=\"wp-block-image size-full\"><img loading=\"lazy\" decoding=\"async\" width=\"703\" height=\"651\" src=\"https:\/\/gaviki.com\/blog\/wp-content\/uploads\/2025\/06\/image-69.png\" alt=\"\" class=\"wp-image-27354\" srcset=\"https:\/\/gaviki.com\/blog\/wp-content\/uploads\/2025\/06\/image-69.png 703w, https:\/\/gaviki.com\/blog\/wp-content\/uploads\/2025\/06\/image-69-300x278.png 300w\" sizes=\"auto, (max-width: 703px) 100vw, 703px\" \/><\/figure>\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>The compound with the <strong>highest boiling point<\/strong> among the given structures is the <strong>second compound<\/strong>:<\/p>\n\n\n\n<p><strong>CH\u2083CH\u2082\u2013CH(OH)\u2013CH\u2082CH\u2083<\/strong><\/p>\n\n\n\n<h3 class=\"wp-block-heading\">Correct Answer: The <strong>second<\/strong> compound (alcohol group \u2013OH)<\/h3>\n\n\n\n<h3 class=\"wp-block-heading\">Explanation:<\/h3>\n\n\n\n<p>Boiling point is largely influenced by <strong>intermolecular forces<\/strong>. The stronger the forces between molecules, the more energy (and thus a higher temperature) is needed to separate them into the gas phase. Let&#8217;s examine the intermolecular forces present in each compound:<\/p>\n\n\n\n<hr class=\"wp-block-separator has-alpha-channel-opacity\"\/>\n\n\n\n<h4 class=\"wp-block-heading\">1. <strong>CH\u2083CH\u2082\u2013CH(CH\u2083)\u2013CH\u2082CH\u2083<\/strong><\/h4>\n\n\n\n<ul class=\"wp-block-list\">\n<li>This is a branched alkane.<\/li>\n\n\n\n<li>It exhibits only <strong>London dispersion forces<\/strong>, which are the weakest.<\/li>\n\n\n\n<li><strong>Lowest boiling point<\/strong> among the options.<\/li>\n<\/ul>\n\n\n\n<hr class=\"wp-block-separator has-alpha-channel-opacity\"\/>\n\n\n\n<h4 class=\"wp-block-heading\">2. <strong>CH\u2083CH\u2082\u2013CH(OH)\u2013CH\u2082CH\u2083<\/strong><\/h4>\n\n\n\n<ul class=\"wp-block-list\">\n<li>This is a <strong>secondary alcohol<\/strong>.<\/li>\n\n\n\n<li>It exhibits <strong>hydrogen bonding<\/strong>, which is the strongest type of intermolecular force among the options here.<\/li>\n\n\n\n<li>Therefore, this compound will have the <strong>highest boiling point<\/strong>.<\/li>\n<\/ul>\n\n\n\n<hr class=\"wp-block-separator has-alpha-channel-opacity\"\/>\n\n\n\n<h4 class=\"wp-block-heading\">3. <strong>CH\u2083CH\u2082\u2013CH(Cl)\u2013CH\u2082CH\u2083<\/strong><\/h4>\n\n\n\n<ul class=\"wp-block-list\">\n<li>This is a <strong>chloroalkane<\/strong>.<\/li>\n\n\n\n<li>Chlorine is electronegative, so it introduces <strong>dipole-dipole interactions<\/strong>, which are stronger than London forces but weaker than hydrogen bonding.<\/li>\n\n\n\n<li>Moderate boiling point.<\/li>\n<\/ul>\n\n\n\n<hr class=\"wp-block-separator has-alpha-channel-opacity\"\/>\n\n\n\n<h4 class=\"wp-block-heading\">4. <strong>CH\u2083CH\u2082CH\u2082\u2013O\u2013CH\u2082CH\u2083<\/strong><\/h4>\n\n\n\n<ul class=\"wp-block-list\">\n<li>This is an <strong>ether<\/strong>.<\/li>\n\n\n\n<li>It has dipole-dipole interactions due to the oxygen, but it does <strong>not<\/strong> form hydrogen bonds as there is no \u2013OH group.<\/li>\n\n\n\n<li>Boiling point is higher than alkanes, but lower than alcohols.<\/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\">Conclusion:<\/h3>\n\n\n\n<p>Because of the presence of a hydroxyl (\u2013OH) group that enables <strong>hydrogen bonding<\/strong>, the <strong>second compound<\/strong> (CH\u2083CH\u2082\u2013CH(OH)\u2013CH\u2082CH\u2083) has the <strong>strongest intermolecular forces<\/strong> and hence the <strong>highest boiling point<\/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-banner8-157.jpeg\" alt=\"\" class=\"wp-image-27355\" srcset=\"https:\/\/gaviki.com\/blog\/wp-content\/uploads\/2025\/06\/learnexams-banner8-157.jpeg 852w, https:\/\/gaviki.com\/blog\/wp-content\/uploads\/2025\/06\/learnexams-banner8-157-250x300.jpeg 250w, https:\/\/gaviki.com\/blog\/wp-content\/uploads\/2025\/06\/learnexams-banner8-157-768x923.jpeg 768w\" sizes=\"auto, (max-width: 852px) 100vw, 852px\" \/><\/figure>\n","protected":false},"excerpt":{"rendered":"<p>Which compound will have the highest boiling point? CH3CH2CH2CH2OH CH3CH2CH2CH2Cl CH3CH2CH=CHCH3 CH3CH2CH2CH2OCH2CH3 The Correct Answer and Explanation is: The compound with the highest boiling point among the given structures is the second compound: CH\u2083CH\u2082\u2013CH(OH)\u2013CH\u2082CH\u2083 Correct Answer: The second compound (alcohol group \u2013OH) Explanation: Boiling point is largely influenced by intermolecular forces. The stronger the forces [&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-27353","post","type-post","status-publish","format-standard","hentry","category-quiz-questions"],"_links":{"self":[{"href":"https:\/\/gaviki.com\/blog\/wp-json\/wp\/v2\/posts\/27353","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=27353"}],"version-history":[{"count":1,"href":"https:\/\/gaviki.com\/blog\/wp-json\/wp\/v2\/posts\/27353\/revisions"}],"predecessor-version":[{"id":27356,"href":"https:\/\/gaviki.com\/blog\/wp-json\/wp\/v2\/posts\/27353\/revisions\/27356"}],"wp:attachment":[{"href":"https:\/\/gaviki.com\/blog\/wp-json\/wp\/v2\/media?parent=27353"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/gaviki.com\/blog\/wp-json\/wp\/v2\/categories?post=27353"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/gaviki.com\/blog\/wp-json\/wp\/v2\/tags?post=27353"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}