ALCOHOLS Flashcards

1
Q

what are alcohols

A

compounds with OH group (hydroxyl)

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

when naming alcohols, what is the same consistent first step

A

choosing the parent, identify the longest chain that includes the carbon connected to the -OH group

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

what is the alcohol suffix

A

-ol

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

what is phenol

A

It has an -OH group attached directly to a phenyl ring.

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

what can a phenol be used to identify specifically

A

A phenol can specifically be used to identify hydroxybenzene

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

what is the boiling point of alcohol compared to other hydrocarbons

A

higher compared to alkane counterparts

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

why is the boiling point of alcohols higher than its alkane counterparts

A

they have O-H bonding

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

how can the acidity of a compound be determined

A

look at stability of conjugate base - more stable conjugate base the great the acidity

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

what are alcohols more acidic than

A

alkanes

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

why are alcohols more acidic than alkanes

A

the negative charge on the oxygen is more stable than the negative charge on a carbon

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

what is the conjugate base of alcohol called

A

alkoxide ion [neg charge]

R – O-

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

what two factors affect the acidity of an alcohol [when selecting between structures]

A

Resonance
Induction

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

how does resonance affect the acidity of an alcohol

A

if resonance present > acidity is greater

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

how does induction affect acidity of an alcohol

A

the more electronegative atoms in the alcohol - the more acidic it is

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

what is the property of electronegative atoms

A

they can attract a negative charge toward them so conjugate base is stabilise

electron-withdrawing substituent can increase acidity of nearby atom aka alcohol

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

list the electronegative atoms that would make alcohol most acidic from most electronegative to least electronegative in an alcohol

A

F
Cl
Br
I

17
Q

in induction/electronegativity, what conditions are more likely to make an alcohol more or less acidic

A

distance between the electronegative element and the negative charge on the O in the conjugate base

18
Q

what is a Grignard reagent

A

alkyl halide + magnesium

R-Mg-X

19
Q

Why is a C-MG bond so significant

A

Carbon and magnesium have such a great difference in electronegativity that the bond between them can be treated as separate charges

20
Q

how does the Grignard reagent act

A

as a nucleophile

21
Q

how does the carbon nucleophile act

A

it can attack range of electrophiles including carbonyl group of ketones and aldehydes [C=O]

22
Q

what happens if the Grignard reaction attacks the carbonyl group of a compound

A
  1. Gringard reagent acts as nucleophile and attacks carbonyl group
  2. Causes proton to be transferred from R-Mg-X to alkoxide ion on compounds
  3. Forms an alcohol