reaction conditions and types Flashcards

1
Q

conditions to convert a alkene to a poly(alkene)

A

-high pressure,
-catalyst

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2
Q

condition and mechanism to convert an alkene to a dihalogenoalkane

A

-Br2 or Cl2,
-room temperature,
mechanism- electrophilic addition

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3
Q

condition and mechanism to convert dihalogenoalkane to a diol

A

-aqueous KOH,
-heat under reflux
mechanism- nucleophilic substitution

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4
Q

conditions to covert an alkene to an alcohol

A

1- add H2SO4
mechanism electrophilic addiction
2- H2O, warm
mechanism- hydrolysis

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5
Q

conditions to convert an alcohol to an alkene

A

-concentrated H2SO4 or concentrated H3PO4
mechanism- elimination (dehydration)

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6
Q

conditions to convert an alcohol (primary) to an aldehyde

A

-acidified potassium dichromate
-heat and distill
-(partial) oxidation

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7
Q

conditions to convert an alcohol (secondary) to a ketone

A

-acidified potassium dichromate
-heat and distill
-oxidation

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8
Q

conditions to convert an aldehyde to a alcohol

A

-NaBH4
-reduction
-nucleophilic addiction

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9
Q

conditions to convert an aldehyde to a carboxylic acid

A

-acidified potassium dichromate
-reflux in excess oxidising agent
-oxidation

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10
Q

conditions to convert an aldehyde to a hydroxynitrile

A

-HCN or NaCN
-H2SO4
-nucleophilic addition

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11
Q

conditions to convert a ketone to an alcohol

A

-NaBH4
-reduced
-nucleophilic addition

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12
Q

conditions to convert a ketone to a hydroxynitrile

A

-HCN or NaCN
-H2SO4
-nucleophilic addition

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13
Q

conditions to convert a carboxylic acid to an ester

A

-alcohol
-H2SO4
-heat
-esterification

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14
Q

conditions to convert an alcohol to an ester

A

-carboxylic acid
-H2SO4
-heat
-esterification

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15
Q

conditions to convert an acyl chloride or acid anhydride to an ester

A

-alcohol
-room temperature
-nucleophilic addition elimination

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16
Q

conditions to convert an acyl chloride or an acid anhydride to a carboxylic acid

A

-H2O
-room temperature
-nucleophilic addition elimination

17
Q

conditions to convert an acyl chloride or an acid anhydride to a primary amide

A

-NH3
-room temperature
-nucleophilic addition elimination

18
Q

conditions to convert an acyl chloride or an acid anhydride to a secondary amide

A

-primary amine
-room temperature
-nucleophilic addition elimination

19
Q

conditions to convert a primary amide to a secondary amide

A

-acyl chloride
-room temperature
-nucleophilic addition elmination

20
Q

conditions to convert a conditions to convert a primary amide to a secondary to tertiary amide or a quaternary salt

A

-halogenoalkane
-nucleophilic substitution

21
Q

conditions to convert a nitrile to a primary amine

A

-LiAlH4 and dry ether
-dilute acid
or H2 and Ni catalyst
-high temperature and pressure
-reduction

22
Q

conditions to convert a halogenoalkane to a nitrile

A

-KCN in ethanol
-water mixture
-heat under reflux
-nucleophilic substitution

23
Q

conditions to convert a halogenoalkane to a primary amine

A

-alcoholic NH3
-heat under pressure
-nucleophilic substitution

24
Q

conditions to convert a halogenoalkane to an alcohol

A

-KOH aqueous
-heat under reflux
-nucleophilic substitution

25
conditions to convert a halogenoalkane to an alkene
-KOH alcoholic -heat under reflux -elimination
26
conditions to convert an alkene to a halogenoalkane
-HBr or HCl -room temperature -electrophilic addition
27
conditions to convert an alkane to a halogenoalkane
-Br2 or Cl2 -UV light -free radical substitution
28
conditions to convert benzene to a phenylketone
-RCOCl -AlCl3 catalyst -reflux -non-aqueous environment -acylation
29
conditions to convert benzene to nitrobenzene
-Conc H2SO4 (catalyst) -Conc HNO3 -below 55 degrees -nitration NO2+ (+ on N not O) genetated by HNO3 + H2SO4 --> NO2+ + HSO4- + H2O
30
conditions to convert nitrobenzene to phenylamine
-Sn -Conc HCl -reflux -NaOH -reduction
31
conditions to convert phenylamine to N-phenylethanamide
-CH3COCl -25 degrees -addition elimination
32
conditions to convert a halogenoalkane to a nitrile
-reagent KCN -condition aqueous and ethanol