reactions Flashcards

1
Q

reagents and conditions for alkene -> alkane

A

H2/Ni
150’

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

reagents and conditions for alkene -> dihalogenoalkane

A

X2
room temp

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

reagents and conditions for alkane -> halogenoalkane

A

Cl2
UV

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

reagents and conditions for alkene -> halogenoalkane

A

HX

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

reagents and conditions for halogenoalkane -> alkene

A

NaOH + ethanol
heat

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

reagents and conditions for halogenoalkane -> alcohol

A

NaOH(aq)

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

reagents and conditions for alcohol -> halogenoalkane

A

conc HX/PCL5

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

reagents and conditions for alcohol -> ketone

A

2’ alcohol + acidified potassium dichromate
reflux

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

reagents and conditions for alcohol -> aldehyde

A

1’ alcohol + acidified potassium dichromate
distill out immediately

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

reagents and conditions for ketone -> alcohol

A

LiAlH2 + ethoxyethane
hydrolysis

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

reagents and conditions for aldehyde -> alcohol

A

LiAlH2 + ethoxyethane
hydrolysis

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

reagents and conditions for aldehyde -> hydroxynitrile

A

KCN + HCN

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

reagents and conditions for ketone -> hydroxynitrile

A

KCN + HCN

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

reagents and conditions for Grignard reagent -> 1’ alcohol

A

HCOH

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

reagent and conditions for Grignard reagent -> 2’ alcohol

A

RCOH

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

reagent and conditions for Grignard reagent -> 3’ alcohol

A

RCOR’

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

reagent and conditions for halogenoalkane -> Grignard reagent

A

Mg + ethoxyethane

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

reagents and conditions for halogenoalkane -> amine

A

conc NH3 + ethanol

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

reagents and conditions for halogenoalkane -> nitrile

A

KCN + ethanol

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
20
Q

reagents and conditions for nitrile -> amine

A

H2/Ni
150’

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
21
Q

reagents and conditions for Grignard reagent -> carboxylic acid

A

CO2
hydrolysis

22
Q

reagents and conditions for nitrile -> carboxylic acid

23
Q

reagents and conditions for carboxylic acid -> aldehyde

A

LiAlH2 + ethoxyethane
hydrolysis

24
Q

reagents and conditions for aldehyde -> carboxylic acid

A

acidified potassium dichromate
reflux

25
reagents and conditions for carboxylic acid -> ester
ROH + conc H2SO4 heat
26
reagents and conditions for ester -> carboxylic acid
HCl(aq) /H2SO4(aq) reflux
27
reagents and conditions for carboxylic acid -> acylchloride
PCl5 room temp
28
reagents and conditions for acylchloride -> carboxylic acid
H2O room temp
29
reagents and conditions for acylchloride -> ester
ROH room temp
30
reagents and conditions for acylchloride -> amide
conc NH3
31
what reaction(s) forms an amide
acylchloride undergoes a condensation reaction with concentrated ammonia
32
what reaction(s) forms an ester
nucleophillic substitution-elimination of an acyl chloride with ROH at room temperature esterfication of a carboxylic acid when heated with ROH and concentrated H2SO4
33
what reaction(s) form a carboxylic acid
hydrolysis of acylchloride with H2O at room temperature hydrolysis of an ester with concentrated HCl(aq) or H2SO4(aq) under reflux oxidation of aldehyde/1' alcohol with acidified potassium dichromate under reflux hydrolysis of a nitrile with HCl(aq) and heat Grignard reagent + CO2 then hydrolysis with water
34
what reaction(s) form an acylchloride
carboxylic acid + PCl5 at room temperature
35
what reaction(s) form a nitrile
nucleophilic substitution of a halogenoalkane with KCN + ethanol
36
what reaction(s) form an amine
nucleophilic substitution of halogenoalkane + concentrated ammonia (NH3) and ethanol in a sealed container nitrile + H2/Ni at 150'
37
what reaction(s) form a Grignard reagent
halogenoalkane + Mg and ethoxyethane (dry ether)
38
what reaction(s) form a halogenoalkane
free radical substitution of an alkane to a halogenoalkane with Cl2 and uv light electrophilic addition of alkene with HX substitution of an alcohol with concentrated HX or PCl5
39
what reaction(s) form an alkane
hydrogenation of an alkene with H2/Ni at 150'
40
what reaction(s) form an alkene
elimination reaction of a halogenoalkane by heating with NaOH and ethanol
41
what reaction(s) form a dihalogenoalkane
alkene + X2 at room temperature
42
what reaction(s) form an alcohol
hydrolysis of a halogenoalkane with NaOH(aq) Grignard reagent + HCOH + RCHO + R'COR'' and hydrolysis reduction of a ketone using LiAlH4 + ethoxyethane (dry ether) and hydrolysis reduction of an aldehyde using LiAlH4 + ethoxyethane (dry ether) and hydrolysis
43
what reaction(s) form a ketone
oxidation of a 1' alcohol with acidified potassium dichromate(VII) under reflux
44
what reaction(s) form an aldehyde
oxidation of a 2' alcohol with acidified potassium dichromate(VII) and distill out immediately reduction of a carboxylic acid with LiAlH4 + ethoxyethane (dry ether) and hydrolysis
45
what reaction(s) form a hydroxynitrile
ketone/aldehyde + KCN + HCN
46
what are the reagents and conditions for benzene -> chlorobenzene
Cl2(g) + AlCl3 room temperature substitution
47
what are the reagents and conditions for benzene -> nitrobenzene
conc H2SO4/HNO3 55' substitution
48
what are the reagents and conditions for nitrobenzene -> phenylamine
tin + conc HCl reflux reduction
49
what are the reagents and conditions for benzene -> benzeneCOR
RCOCl/(RCO)2O + AlCl3 reflux Friedel crafts acylation
50
what are the reagents and conditions for benzene -> methylbenzene
RCl + AlCl3 reflux Friedel crafts alkylation
51
what are the reagents and conditions for benzene -> benzenesulfonic acid
conc H2SO4 reflux substitution
52
what are the reagents and conditions for benzene -> bromobenzene
Br2 + FeBr3/Fe room temperature substitution