Unit 1 Flashcards

(38 cards)

1
Q

Alkane/ ene/ yne polarity

A

Non polar

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

Alkane/ ene/ yne main intermolecular force

A

London dispersion

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

Alkane/ ene/ yne Mp/Bp

A

Low but get higher as the chain gets longer

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

Organic Halides polarity

A

More polar than hydrocarbons which means higher mp/ bp and more soluble. The more halogens there are, the more polar it gets

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

Alcohols polarity

A

Polar, they form hydrogen bonds so higher mp/ bp

Short chain alcohols are good polar solvents

Long chain alcohols are good polar and non polar solvents

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

Ethers polarity

A

Can not form hydrogen bonds but the oxygen makes it more polar than alkanes

Good as a polar and non polar solvent because it is very chemically stable

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

Aldehydes and ketones polarity

A

Both polar and non polar, good solvents. Less soluble in water that alcohol because there is no hydrogen bonding

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

Ethers mp/bp

A

Mp/ bp is higher than alkanes but lower that alcohols and water

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

Aldehydes and ketones mp/ bp

A

Lower than alcohols

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

Carboxylic acids polarity

A

Polar and form hydrogen bonds
Similar solubilities to alcohols
Behave like other acids

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

Carboxylic acids mp/bp

A

higher mp/bp than alcohols

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

Which side of esters goes first

A

Carboxylic acid

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

Ester polarity

A

Less polar than the parent acid and alcohol which leads to lower mp/ bp

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

Ester at room temp

A

Gasses. Lower molecular mass

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

Amines mp/bp

A

Higher than alkanes

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

Amines solubility

A

Smaller molecules are more soluble

17
Q

Amines smell

18
Q

Amines Types of bonds

A

Hydrogen bonds

19
Q

Amines Bond polarity

20
Q

Amides properties

A

Weak bases, H+ receivers

21
Q

Amides solubility

A

Not soluble in water

22
Q

Amides Mp/ bp

A

If alkyl group is on the end they have lower mp/bp that if NH2 group is on the end

23
Q

Addition polymers

A

linkage by unsaturated carbon bonds

24
Q

Polyesters

A

Made from a dicarboxylic acid and a diol

25
Polyamides
Made from an anime group and a carboxylic acid
26
Alkanes substitution
Br2 turns into HBr
27
Halogenation
Br2 breaks a double bond
28
Hydrogenation
H2 breaks a bond (needs to be balanced)
29
Hydrohalogenation
HBR breaks double bonds
30
Hydration
H2O is used to form am alcohol
31
Elimination (organic halides)
Strong acid or base is used to remove a halogen
32
Dehydration (alcohols)
Alcohol turns into water and an alkene
33
Condensation (ethers)
How an ether is formed
34
Synthesis (A+K)
Aldehydes and keynote are formed
35
Esterification
An ester is formed
36
Hydrolysis/ saponificantion
A carboxylic acid and alcohol are formed from an ester
37
Synthesis (amides)
Adding NH3 to a carboxylic acid
38
Hydrolysis (amides)
Breaks them apart