idk yet Flashcards

1
Q

What is non-superimposable?

A

Can’t place one directly on top of the other and them be the same

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2
Q

What is a chiral carbon?

A

A carbon with 4 different groups

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3
Q

What are the mirror images called in an optical isomer?

A

Enantiomers

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4
Q

What is a racemic mixture?

A

50:50 split of both enantiomers

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5
Q

How do you test for optical isomers?

A

Using a polarised light filter
-depending on the enantiomer, will rotate the light clockwise or anti-clockwise.

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6
Q

Aldehyde or ketone goes to alcohol, what is the mechanism called?

A

Nucleophilic addition

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7
Q

What is the conditions for nucleophilic addition?

A

Slightly acidic

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8
Q

What mechanism can form optical isomers?

A

nucleophilic addition

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9
Q

Why can optical isomers be formed from nucleophilic addition?

A

The carbonyl is planar so the nucleophile can attack from either side to make a chiral carbon, so equal liklihood, racemic mixture

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10
Q

Why might an optical isomer not be formed?

A

Ketone was symmetrical

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11
Q

What is the reducing agent for ketones and aldehydes?

A

Sodium borohydride - NaBH4

[H]
:H-

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12
Q

What is Sodium Borohydride represented as in a mechanism for ketone reduction?

A

-:H

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13
Q

Why is the boiling points of carboxylic acids high?

A

More VDW forces as it forms a dimer, double hydrogen bonding between The H of OH and O of C=O

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14
Q

What forces do esters have?

A

VDW and dipole-dipole

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15
Q

Can an ester react as an acid?

A

No

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16
Q

What makes an ester?

A

Alcohol + Carboxylic acid ——> (reversible) ester

Reflux and strong sulphuric acid catalyst

17
Q

How do you name an ester?

A

Alcohol= side chain
Carboxylic acid= main name

Methanol + ethanoic acid. —-> Methyl ethanoate

18
Q

Describe the structure of an ester

A

C=O bonded with another O and two R groups

19
Q

What might esters be used for in life?

A

Solvents, sweet smells, foods

20
Q

What can you hydrolyse an eater with!

A

Acidic: H2O
Alkaline: NaOH

21
Q

Describe the transesterification reaction

A

Oil + Methanol (3CH3OH) ——-> glycerol + CH3OOCH

22
Q

What is an anhydride?

A

Form a W shape C=O O C=O
and R groups

23
Q

What is an Acyl Chloride?

A

R group with C=O and Cl

24
Q

How do you name an acyl chloride?

A

longest carbon chain + oyl chloride

e.g ethanoyl chloride

25
Q

What do you use Nucleophilic Addition Elimination for?

A

Acyl chlorides

Add water, eliminates Cl into OH
Leaves alcohol and HCl

26
Q

Why are acid anhydrides better than acid chlorides?

A

Cheaper
Less corrosive
Doesn’t react readily with water
Safer
Don’t need as much

Slower tho

27
Q

How do you name an acid anhydride?

A

Name one of the carboxylic acids in it, change oic acid to oic anhydride