25. Quartenary ammonium salts with hydrocarbon chains are used as detergent BECAUSE the presence of hydrophobic tail and ionic head facilitates its detergent action. 26. Hofmann elimination is a reaction between an unsubstituted amide and an alkaline solution of bromine BECAUSE the advantage of Hofmann rearrangement is that it yields pure primary amines 27. Nitriles undergo catalytic hydrogenation or reduction with LIAIH4 to yield primary amines BECAUSE this reaction is a technique for shortening carbon chain in an amine.

Organic Chemistry
9th Edition
ISBN:9781305080485
Author:John E. McMurry
Publisher:John E. McMurry
Chapter22: Carbonyl Alpha-substitution Reactions
Section22.SE: Something Extra
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State whether false or true

25. Quartenary ammonium salts with hydrocarbon chains are used as detergent
BECAUSE the presence of hydrophobic tail and ionic head facilitates its
detergent action.
26. Hofmann elimination is a reaction between an unsubstituted amide and an
alkaline solution of bromine BECAUSE the advantage of Hofmann
rearrangement is that it yields pure primary amines
27. Nitriles undergo catalytic hydrogenation or reduction with LIAIH4 to yield
primary amines BECAUSE this reaction is a technique for shortening carbon
chain in an amine.
Transcribed Image Text:25. Quartenary ammonium salts with hydrocarbon chains are used as detergent BECAUSE the presence of hydrophobic tail and ionic head facilitates its detergent action. 26. Hofmann elimination is a reaction between an unsubstituted amide and an alkaline solution of bromine BECAUSE the advantage of Hofmann rearrangement is that it yields pure primary amines 27. Nitriles undergo catalytic hydrogenation or reduction with LIAIH4 to yield primary amines BECAUSE this reaction is a technique for shortening carbon chain in an amine.
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