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Solution: Ketones on reduction with magnesium amalgum and water form pinacols. Ketones upon reaction with Grignard regent from tertiary-alcohol. Formaldehyde with Grignard reagent forms primary alcohol, acetaldehyde with Grignard reagent forms secondary alcohol. 2∘ alcohol (except formaldehyde which form 1∘ alcohol).
Mechanism This mechanism is for a LiAlH 4 reduction. The mechanism for a NaBH 4 reduction is the same except methanol is the proton source used in the second step. 1) Nucleophilic attack by the hydride anion 2) The alkoxide is protonated Going from Reactants to Products Simplified Properties of hydride sources
Solution The correct option is C Ethyl benzene Suggest Corrections 1 Similar questions Q. Acetophenone on reduction with Zn/Hg in the presence of HCl gives Q. Acetophenone is reduced by LiAlH4 to Q. Acetone on reaction with Zn (Hg), HCl gives Q. Benzene reacts with 1 equivalent of CH3Cl in the presence of anhydrous AlCl3 to form
18/11/2021· Welcome to Sarthaks eConnect: A unique platform where students can interact with teachers/experts/students to get solutions to their queries. Students (upto class 10+2) …
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