Nitrogen compounds Flashcards

Amines, Amides & Nitrile reaction

1
Q

What is an Amine?

A

Compounds where one or more of the Hs on ammonia(NH3) are replaced by an alkyl chain

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

How are aliphatic amines made?

A

Alkyl + Ammonia in a sealed tube as ammonia is volatile, and would escape otherwise

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

How are aromatic amines made?

Phenylamine

A

By reducing nitrobenzene’s

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Why do amine react with acids?

A

Amines are basic, they accept H+ protons (Bronsted base) / donate electron pairs(Lewis base)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

How do amines form alkylammonium ions?

A

Nitrogen accepts protons/ donates one pair electron to H+ forms R[NH3]+

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

What happens when you reduce a nitrobenzene?

C₆H₅NO₂ + 6[H] →

A

forms Phenylamine & Water

C₆H₅NH₂

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

How do you name amides?

A

alk-anamide

e.g. Methanamide, Ethanamide, Propanamide

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

In secondary & tertiary amides what does the N- attached to alkyl chains represent?

A

The N shows that the alkyl chain is attached to the nitrogen (but isn’t the carbonyl chain)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

What reactions do Nitriles have?

A

Nucleophilic reaction

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

What happens when Nitriles undergo nucleophilic addition?

A

They replace other nucleophile groups like OH- Cl,Br,I that are bonded to carbons

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

What happens when Nitriles react with a carbonyl?

A

They join a carbonyl the C=O double bond breaks with electrons moving to O to from O- which forms an alcohol

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

When are nitriles used in reactions?

A

To extend chain length, the C≡N bond breaks they can make an amine group or sum shit

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

what are the reagents needed for the nucleophilic sub of a Haloalkane to an amine

A

excess ethanolic ammonia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

how to go from nitrile to carboxylic acid

A

Heat with water in Acidic conditions(acid must be included: H20,H+)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Nitrile to amine?

A

Hydrodgenation with nickel catalyst

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

what conditions are needed to go From nitrobenzene TO phenylamine

A

Sn + conc HCL

17
Q

what conditions are needed to nitrate benzene

A

conc HNO3 + conc H2SO4 as catalyst