{"id":19917,"date":"2024-04-15T05:45:58","date_gmt":"2024-04-15T05:45:58","guid":{"rendered":"https:\/\/exam.pscnotes.com\/mcq\/?p=19917"},"modified":"2024-04-15T05:45:58","modified_gmt":"2024-04-15T05:45:58","slug":"the-compound-is-a-aromatic-and-high-dipole-moment-b-aromatic-and-has-no-dipole-moment-c-non-aromatic-and-has-high-dipole-moment-d-anti-aromatic-and-has-no-dipole-moment","status":"publish","type":"post","link":"https:\/\/exam.pscnotes.com\/mcq\/the-compound-is-a-aromatic-and-high-dipole-moment-b-aromatic-and-has-no-dipole-moment-c-non-aromatic-and-has-high-dipole-moment-d-anti-aromatic-and-has-no-dipole-moment\/","title":{"rendered":"The compound is A. aromatic and high dipole moment B. aromatic and has no dipole moment C. non-aromatic and has high dipole moment D. anti-aromatic and has no dipole moment"},"content":{"rendered":"

[amp_mcq option1=”aromatic and high dipole moment” option2=”aromatic and has no dipole moment” option3=”non-aromatic and has high dipole moment” option4=”anti-aromatic and has no dipole moment” correct=”option1″]<\/p>\n

The correct answer is: A. aromatic and high dipole moment.<\/p>\n

Aromatic compounds are cyclic, planar, and conjugated molecules that have a high electron density in the ring. This high electron density results in a strong dipole moment, which is a measure of the separation of charge in a molecule.<\/p>\n

The compound in the question is benzene, which is a classic example of an aromatic compound. Benzene is a planar molecule with a six-membered ring of carbon atoms. The carbon atoms in benzene are sp2 hybridized, which means that they have two p orbitals that are perpendicular to the plane of the ring. These p orbitals overlap to form a pi bond system that is delocalized around the entire ring. This delocalization of electrons results in a high electron density in the ring, which in turn results in a strong dipole moment.<\/p>\n

The dipole moment of benzene is 1.5 D. This is a relatively high dipole moment, which is consistent with the high electron density in the ring.<\/p>\n

The other options are incorrect. Option B is incorrect because benzene is not a non-aromatic compound. Option C is incorrect because benzene does not have a high dipole moment. Option D is incorrect because benzene is not an anti-aromatic compound.<\/p>\n","protected":false},"excerpt":{"rendered":"

[amp_mcq option1=”aromatic and high dipole moment” option2=”aromatic and has no dipole moment” option3=”non-aromatic and has high dipole moment” option4=”anti-aromatic and has no dipole moment” correct=”option1″]<\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[688],"tags":[],"class_list":["post-19917","post","type-post","status-publish","format-standard","hentry","category-basics-of-organic-reaction-mechanism","no-featured-image-padding"],"yoast_head":"\nThe compound is A. aromatic and high dipole moment B. aromatic and has no dipole moment C. non-aromatic and has high dipole moment D. anti-aromatic and has no dipole moment<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" 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