Back to marketplace

Amines (P2+P3)

No description yet. This curated deck is ready for daily study.

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

Card preview (14)

#1
Front (Question)

All amines (NH2) can act as a …

Back (Answer)

base

#2
Front (Question)

Which is stronger Ethylamine or Ammonia?

Back (Answer)

Ethylamine because - the ethyl group releases electron density onto the N - so the lone pair on the N is more available to be protonated.

#3
Front (Question)

Which is stronger Phenylamine or Ammonia?

Back (Answer)

Ammonia because - the lone pair on the N of phenylamine can delocalise into the pi bond of the phenyl ring. - so is less available to accept a proton.

#4
Front (Question)

Give the equation for Ethylamine and Nitric acid and name the compound formed

Back (Answer)

C2H5NH2 + HNO3 –> C2H5NH3NO3 name of compound ethylammonium nitrate.

#5
Front (Question)

To ensure a higher yield of primary amine you would…

Back (Answer)

Use excess ammonia

#6
Front (Question)

What is tetramethyl ammonium chloride and example of?

Back (Answer)

quaternary ammonium salt

#7
Front (Question)

Uses of quaternary ammonium salt include…

Back (Answer)

• hair conditioner • fabric softener

#8
Front (Question)

Further substitution requires…

Back (Answer)

Excess haloalkane

#9
Front (Question)

What are the reagents for reduction of nitriles into amines?

Back (Answer)

Hydrogen and nickel catalyst.

#10
Front (Question)

What are the reagents, conditions and problems associated with nucleophilic substitution to form amines?

Back (Answer)

reagents - NH3 conditions - excess problems - further substitutions.

#11
Front (Question)

What are the reagents, conditions and problems associated with nitrile/reduction to form amines?

Back (Answer)

Nitriles; reagents- KCN conditions - Aq + ethanolic Reduction; reagents - H2 conditions- nickel catalyst problems - KCN is toxic + 2 steps required

#12
Front (Question)

To form phenylamine (NH2) from nitrobenzene (NO2) what are the reagents and conditions needed?

Back (Answer)

reagents- HCl conditions - tin catalyst

#13
Front (Question)

Equation for forming phenylamine from nitrobenzene

Back (Answer)

C6H5NO2 + 6[H] –> C6H5NH2 + 2H2O

#14
Front (Question)

Amines can be used to MAKE…

Back (Answer)

• dyes • drugs