amines Flashcards

1
Q

Amine functional group

A

R-NH2 etc

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2
Q

Amide functional group

A

R-C(=O)-NH2 etc

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3
Q

Aliphatic meaning

A

Non aromatic

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4
Q

Reaction of aliphatic amine
With water

A

Donates hydrogen atom to the NH2 to form an NH3+
Acts as a base
Reversible
Amine acts as base because accepts a proton

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5
Q

Reaction of amine with acid

A

R-NH3+(salt)-

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6
Q

Reaction of acyl chloride and amine

A

Nucleophilic substitution / elimination
Cl from acrylic chloride is remove and H from amine reduced and join to form an amide
Need to know mechanism

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7
Q

Reaction of amine and haloalkane

A

R-X + 2NH3 -> R-NH2 +NH4 X
Nucleophilic substitution
Idk bruv
Forms secondary amine

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8
Q

Reaction of little ammonia with copper 2+ solution

A

[Cu(H2O)6]2+ + 2NH3 -> [Cu(H2O)4(OH)2] + 2NH4+
Reversible bc ammonia is only a weak base
Ppt can be written as Cu(OH)2
Pale blue ppt

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9
Q

Reaction of excess ammonia with copper 2+ solution

A

[Cu(H2O)6]2+ + 4NH3 -> [Cu(NH3)4(H2O)2]2+ + 4H2O
Deep blue solution
Ammonia donates lone pare of electrons

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10
Q

reasons for the difference in basicity of ammonia, primary aliphatic amines

A

Alkyl groups increase basicity because they
- push e- density to the nitrogen atom which makes the nitrogen lone pair more attractive to hydrogen ions.
- stabilise +ve charge on nitrogen after an ion is formed

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11
Q

reasons for the difference in basicity of ammonia and primary aromatic amines

A

Aromatic groups decrease basicity
Benzene ring with draws electron density from nitrogen atom, lone pair is less available for proteins

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12
Q

Production of amine from nitrile

A

reduce with LiALH4 and dry ether
(Or hydrogen gas and metal, nickel, catalyst)

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13
Q

Reaction of aromatic nitro compounds

A

Use ting and conc HCl to for amines

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14
Q

Type of reaction when forming polyamide

A

Condensation polymerisation

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15
Q

Molecules which from condensation polymers

A

Dicarboxylic acid and diols
Dicarboxylic acid and diamines
Amino acids

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16
Q

How peptide bonds form

A

Condensation polymerisation of amino acid

17
Q

Hydrolysis of peptide bond

A

Broken into constituent amino acids, can be separated by gas chromatography

18
Q

Chirality of 2-amino acids

A

Contain chiral carbon
Rotate plane polarised light

19
Q

Acidity of amino acids

A

Contain an acidic group (COOH) and basic group (NH2)
Forms a zwitterion
In basic conditions COOH becomes COO-
In acidic conditions NH2 becomes NH3+

20
Q

Ninhydrin

A

Reacts with amino acid to give dark purple colour

21
Q

Reaction of amine with HCl

A

CH3NH2 + HCL -> CH3NH3+ + Cl-