All Of Mechanism Flashcards

1
Q

Alkane to haloalkane

A

Free radical substitution
Uv light needed to break halogen halogen bond
4 stages

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2
Q

Free radical mechanism

A

IPT
1. Initiation
Diatomic molecule forms 2 free radicals
2. Propagation 1
Form a halogen halide and free radical
3. Propagation 2
Form a free radical and haloalkane
4. Termination
Any 2 free radicals combine

Overall equation
CH4 + 3F2 = CH3F3 + 3HF
LOOK AT ORGINAL MOLECULES AND NUMBER OF F3 AND BALANCE WITH 3

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3
Q

Haloalkane to alcohol

A

Name of mechanism = nucleophilic substitutions
Reagent = NaOH/KOH
Condition = aqueous solvent

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4
Q

Haloalkane to nitrile

A

(C=N)
Name of mechanism = nucleophilic substitutions
Reagent = KCN
Condition = water and ethanol solvent

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5
Q

Haloalkane to amine

A

NH2
Name of mechanism = nucleophilic substitutions
Reagent = excess NH3
Condition= ethanol solvent , heat and pressure
1st NH3 = nucleophile( electron pair donor )
2nd NH3 = base ( proton acceptor )

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6
Q

Haloalkane to Alkene

A

Name of mechanism= elimination
Reagent = NaOH ( base )
Condition = ethanolic solvent

OH with lone attracted to H on either side of carbon with halogen
Forms H2O And br -
Forms E/Z isomers

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7
Q

Alkene to haloalkane

A

Name of mechanism= electrophilic addition
Reagent = Hbr
Condition = none as alkenes are very reactive
Take into account which carbocation
Forms major and minor products

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8
Q

Alkene to haloalkane

A

Name of mechanism= electrophilic addition
Reagent = br2
Condition =none
Explain why bromine reacts with alkenes even though it’s non polar ?
Alkenes are electron rich in the pi bond this induces a dipole in br2 pushing the electrons further back the delta positive bromine is attracted to Caron double bond

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9
Q

Alkene to haloalkane

A

Name of mechanism= electrophilic addition
Reagent = H2SO4
Condition = none

Forms a ..yll hydrogen sulfate and can further produce an alcohol

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10
Q

Alkyl hydrogen sulfate = alcohol

A

H2SO4 catalyst
H2O used
Condition = heat

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11
Q

Alkene to alcohol

A

Name of mechanism= direct hydration
Reagent = H2O
Condition = hot concentrated H3PO4/H2SO4
Use H+ first ( arrow to H+)
Use H2O with lone pair attracted to c+

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12
Q

Alcohol = Alkene

A

Name of mechanism= dehydration / elimination
Condition = Hot concentrated H2SO4
Forms H2O and H+

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13
Q

Nitrile to amine

A

Name of mechanism= reduction
Reagent = H2
Condition = nickel catalyst

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14
Q

Complete combustion

A

Uses O2
Produces H2O and CO2

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15
Q

Incomplete combustion

A

Uses O2
Produces H2O + c/CO

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16
Q

Primary alcohol to aldehyde

A

Name of mechanism= oxidation
Reagent = acidified potassium dichromate
Condition = heat under distillation
1(O) used 1H2O produced

17
Q

Aldehyde to carboxylic acid

A

Name of mechanism= oxidation
Reagent = acidified potassium dichromate
Condition = heat under reflux
1(O) used

18
Q

Primary alcohol to carboxylic acid

A

Name of mechanism= oxidation
Reagent = excess acidified potassium dichromate
Condition = heat under reflux
2 (O) used 1H2O produced

19
Q

Secondary alcohol to ketone

A

Name of mechanism= oxidation
Reagent = acidified potassium dichromate
Condition = heat under distillation or reflux
1(O) used 1H2O produced

20
Q

Glucose to alcohol

A

Name of mechanism= fermentation
Reagent = yeast catalyst
Condition = no air temperature between 35-40

21
Q

Acyl chloride = carboxylic acid

A

H2O
Forms carboxylic and HCl

22
Q

Acyl chloride = ester

A

Alcohol
Produces ester and HCl

23
Q

Acyl chloride= amide

A

Ammonia
Amide (NH2) and NH4Cl

24
Q

Acyl chloride = N substituted amide

A

Amide
Forms RNH3Cl

25
Q

Aldehyde / ketone = alcohol

A

Nucleoplilic addition
NaBH4
H- nucleophile then H+
Acidic solvent needed

26
Q

Aldehyde / ketone = hydroxy nitrile

A

Nucleophilic addition
KCN
Acidic solvent needed
CN then H+