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Amines

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Total cards: 14•Content version: v4•Public deck•Updated: 8/1/2026

Card preview (14)

#1
Front (Question)

What are amines ?

Back (Answer)

Organic derivatives of ammonia with one or more alkyl or aryl groups bonded to nitrogen atom

#2
Front (Question)

What is the shape of ammonia ?

Back (Answer)

Slightly distorted tetrahedral shape

#3
Front (Question)

In ammonia what occupies one of the tetrahedral positions ?

Back (Answer)

A lone pair of non bonding electrons

#4
Front (Question)

What is the hybridization of nitrogen in ammonia ?

Back (Answer)

Sp3 hybridization

#5
Front (Question)

What are amines classified as ?

Back (Answer)

Primary Secondary Tertiary

#6
Front (Question)

What are quaternary ammonium salts ?

Back (Answer)

They have four alkyl or aryl bonds to a nitrogen atom that bears a positive charge

#7
Front (Question)

Is an amine an electrophile or neucleophile?

Back (Answer)

Nucleophile

#8
Front (Question)

Why is an amine a Lewis base ?

Back (Answer)

Because it’s lonely pair of non bonding electrons can form a bond with an electrophile

#9
Front (Question)

Why can an amine act as a bronsted Lowry base ?

Back (Answer)

Because it can accept a proton from a proton acid

#10
Front (Question)

Why are arylamines weaker bases than simple aliphatic amines?

Back (Answer)

Card back image
#11
Front (Question)

What reaction do amines undergo easily ?

Back (Answer)

Oxidation

#12
Front (Question)

How is air oxidation of amines prevented?

Back (Answer)

Converting the amines to their salts for storage or use as medicine

#13
Front (Question)

How is diazonium formed ?

Back (Answer)

Primary amines react with nitrous acid via the nitrosonium ion to give diazonium cations

#14
Front (Question)

Card front image
Back (Answer)

Azo linkage