mechanisms Flashcards

1
Q

addition polymerisation (free radical)

A

conditions- low temp, high pressure
forms- polyalkene

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2
Q

free radical substitution

A

reagent- Cl2
conditions- UV light
forms- chloroalkane

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3
Q

electrophilic addition (forming a bromoalkane)

A

reagent- HX(g)
conditions- room temp
forms- bromoalkane

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4
Q

electrophilic addition (forming a dibromoalkane)

A

reagent- Br2 in H2O/ organic solvent
conditions- room temp
forms- dibromoalkane

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5
Q

electrophilic addition (with H2SO4)

A

reagent- conc H2SO4
conditions- cold
forms- alkylhydrogensulphate

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6
Q

hydrolysis

A

reagent- water
conditions- warm
forms- alcohol from alkylhydrogensulphate

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7
Q

hydration

A

reagent- steam
conditions- 300c, 60 atm, H3PO4 catalyst
forms- alcohol from alkene

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8
Q

nucleophilic substitution (forming alcohol)

A

reagent- NaOH (aq) or KOH (aq)
conditions- aq, warm, reflux
forms- alcohol from haloalkane

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9
Q

nucleophilic substitution (forming a nitrile)

A

reagent- KCN
conditions- aq, ethanol, boil under reflux
forms- nitrile from haloalkane

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10
Q

nucleophilic substitution (forming an amine)

A

reagent- ammonia
conditions- ethanolic, heat
forms- amine from haloalkane

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11
Q

mild oxidation (primary alcohol)

A

reagent- K2Cr2O7, dilute H2SO4
conditions- warm, distillation
forms- aldehyde from primary alcohol

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12
Q

elimination (using haloalkane)

A

reagent- KOH
conditions- ethanolic, heat
forms- alkene from haloalkane

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13
Q

oxidation (secondary alcohol)

A

reagent- KRCr2O7, dilute H2SO4
conditions- heat, distillation
forms- ketone from secondary alcohol

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14
Q

oxidation (aldehyde)

A

reagent- K2Cr2O7, dilute H2SO4
conditions-heat, reflux
forms- carboxylic acid from aldehyde

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15
Q

elimination (using alcohol)

A

reagent- conc H2SO4
conditions- heat
forms- alkene from alcohol

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16
Q

Fermentation

A

reagent- yeats
conditions- 35-55c, anaerobic
forms- ethanol from glucose