Question 15Consider the mechanism for the conversion below and identify the intermediates that lead to the product.H3O*+ CH,OHOHOCH,EO.OHOH HOOnly A, B, and D are formed.Only B, C, and E are formed.Only A, C, D, and E are formed.Only A, B, C, and D are formed.

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Question 15 Consider the mechanism for the conversion below and identify the intermediates that lead to the product H3O* + CH,OH OH OCH, E OH OH HO Only A, B, and D are formed. Only B, C, and E are formed. Only A, C, D, and E are formed. Only A, B, C, and D are formed.

Question 15 Consider the mechanism for the conversion below and identify the intermediates that lead to the product H3O* + CH,OH OH OCH, E OH OH HO Only A, B, and D are formed. Only B, C, and E are formed. Only A, C, D, and E are formed. Only A, B, C, and D are formed.

EBK A SMALL SCALE APPROACH TO ORGANIC L

4th Edition

ISBN:9781305446021

Author:Lampman

Publisher:Lampman

Chapter35: Sonogashira Coupling Of Iodosubstituted Aromatic Compounds With Alkynes Using A Palladium Catalyst

Section: Chapter Questions

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Diol

In chemistry there are so many chemical compounds that have a hydroxyl group but a chemical compound having two hydroxyl groups (-OH) is termed as a diol. It also implies the presence of two alcohols whereas polyols contain two or more than two hydroxyl groups (-OH). Glycol or 1,2-diol is an aliphatic diol that has two alcohol groups on adjacent carbon atoms. In industries, the most commonly used diol is ethylene glycol.

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