ch27 Flashcards

1
Q

What is the difference between an aliphatic amine and an aromatic amine?

A

Aliphatic - nitrogen is attached to at least one straight or branched carbon chain
Aromatic - nitrogen is attached to an aromatic ring

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2
Q

What do amines often behave as?

A

Bases

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3
Q

How do amines behave as bases?

A

Nitrogen donates electron pair to H+

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4
Q

For the formation of primary amines, what is reacted together in the two steps?

A

Haloalkane and ammonia

Salt and sodium hydroxide

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5
Q

In primary amine formation, what is in excess and why?

A

Ammonia in excess

Prevents product from reacting with more of the haloalkane

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6
Q

In primary amine formation, what is the purpose of ethanol?

A

Solvent

Prevents substitution of haloalkane by water to produce alcohols

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7
Q

What are the two steps of forming a secondary amine from a primary amine?

A

Primary amine + CH3Br and ethanol as solvent

Salt product + NaOH forms secondary amine

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8
Q

How is phenylamine made from nitrobenzene?

A

Nitrobenzene heated under reflux with tin and HCl to form ammonium salt
Ammonium salt reacted with NaOH to produce phenylamine

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9
Q

What do tin and HCl act as in formation of phenylamine from nitrobenzene?

A

Reducing agent

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10
Q

What is the general structure of an alpha amino acid?

A

Carbon attached to four groups: H, R, NH2 and COOH

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11
Q

Which two groups must amino acids contain?

A

Amine

Carboxyl

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12
Q

What is present in ester formation from amino acid?

A

Alcohol + amino acid
H2SO4
NaOH

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13
Q

What is the purpose of NaOH in amino acid esterification?

A

Free the base from the HSO4- salt of H2N- group

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14
Q

Amino acids are amphoteric, what does this mean?

A

Have acidic and basic properties

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15
Q

How can amino acids act as a base and an acid?

A

NH2 group acts as a base

COOH group acts as an acid

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16
Q

How can polyamides be formed from two monomers?

A

dicarboxylic acid + diamine

17
Q

How are amides formed?

A

acyl chloride+ammonia and amines

18
Q

What do optical isomers have in common?

A

found in molecules containing a chiral centre.
chiral centre- carbon attached to 4 different atoms/group of atoms

19
Q

What is optical isomers / enantiomer?

A

non sumperimposable mirror images of eachother

20
Q

What are the two monomer types that form polyesters?

A

alcohol and carboxylic acid
diol and carboxylic acid

21
Q

How can polyesters be formed from one monomer?

A

condensation reaction

22
Q

What is condensation polymerisation?

A

the joining of 2 monomers via condensation reaction ie with elimination of a small molecule like water or HCl

23
Q

What is the common name for polyamides made from two monomers?

23
Q

How can polyamides be formed from just one monomer?

A

containing COOH or acyl chloride and an amine group

24
What is required to undergo acid hydrolysis?
molecule needs to contain a functional group that can be cleaved by water in the presence of an acid catalyst
25
What is formed from polyester undergoing acid hydrolysis?
the original diol and dicarboxylic acid monomers that formed the ester linkage
26
What is required to undergo base hydrolysis?
a water molecule and a base (like NaOH or KOH) to break down the ester or amide linkage
27
What is formed from polyester undergoing acid hydrolysis?
diol and dicarboxylic acid monomers
28
What is formed from acid hydrolysis of polyamide?
a dicarboxylic acid and an ammonium salt of a diamine
29
What is formed from base hydrolysis of polyamide?
the sodium salt of the dicarboxylic acid and the diamine
30
How does addition polymerisation differ from condensation polymerisation with monomers?
monomers contain double bond in addition polymerisation. condensation- 2 monomers with 2 functional groups, 1 monomer with 2 different functional groups
31
How does addition polymerisation differ from condensation polymerisation with backbone?
addition has a backbone of polymer aka continuous chain of carbon condensation- no backbone. polymer contains ester or amide linkage
32
how are polyesters formed
diol + dicarboxylic acid