Interpretation:
It is to be written that the appropriate sequence of equations for each of the given transformation.
Concept introduction:
The alcohols on reaction with thionyl chloride give alkyl chloride.
The nitriles can be prepared by the reaction of
The cyanide (nitrile) can be reduced to a primary
The secondary alcohol on oxidation with strong oxidizing agent chromic acid forms
The cyanohydrin can be prepared by the addition of hydrogen cyanide to carbonyl carbon of
The dehydration of alcohol is the loss of
The primary amine on reaction with alkyl halide gives secondary amine.
The alkyl bromide can be prepared by the reaction of alcohol with phosphorus tribromide
The aqueous ammonia on reaction with
The acetal carbon is the carbon bonded to two alkoxy groups.
The primary alcohol on oxidation with pyridinium dichromate
The cyclic acetal can be hydrolyzed in an acidic condition to form a ketone or aldehyde and corresponding vicinal diol.
The reaction of the secondary amine with an aldehyde or ketone followed by dehydration forms an enamine.
The enamines on catalytic hydrogenation forms tertiary amine.
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- Organic ChemistryChemistryISBN:9781305580350Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. FootePublisher:Cengage Learning