Alphatic Reactions Conditions 2 Flashcards

1
Q

CH2CH2  → CH3CH2Br

A

electrophilic addition using HBr

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2
Q

CH3CH2OH → CH3COOH

A

oxidation using K2Cr2O7(aq) with H2SO4(aq), heat under reflux

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3
Q

CH3CH2Br → CH3CH2OH

A

nucleophilic substitution using KOH(aq) or NaOH(aq), heat under reflux

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4
Q

CH3CH2Br → CH2CH2

A

elimination using KOH in ethanol or NaOH in ethanol

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5
Q

CH3CN → CH3CH2NH2

A

reduction using NaBH4(aq) or LiAlH4 in dry ether followed by HCl(aq)

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6
Q

C6H6 → C6H5CH3

A

electrophilic substitution using CH3Cl and AlCl3 catalyst (Friedel–Crafts reaction)

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7
Q

CH3CHO → CH3CH(OH)(CN)

A

nucleophilic addition using HCN

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8
Q

CH3COOH → CH3COONa+

A

acid–base reaction using NaOH(aq) or NaHCO3(aq)

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9
Q

CH3CH2NH2 → CH3CH2NH3+

A

acid–base reaction using any dilute acid

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10
Q

CH2CH2 → CH3CH2OH

A

hydration using concentrated sulfuric acid followed by dilution with water

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11
Q

CH3COOH → CH3COOCH2CH2CH3

A

esterification (or condensation) using CH3CH2CH2OH with conc. H2SO4 catalyst

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12
Q

Deduce the reaction type from the reagent, then deduce the product.

(conc. H2SO4)

        CH<sub>3</sub>CH<sub>2</sub>OH(l) →   ………………
A

dehydration to CH2CH2 (ethene)

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13
Q

Deduce the reaction type from the reagent, then deduce the product.

(KOH(aq))

        CH<sub>3</sub>CH<sub>2</sub>Br(l)→   ………………
A

nucleophilic substitution to form CH3CH2OH (ethanol)

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14
Q

Deduce the reaction type from the reagent, then deduce the product.

(KOH in ethanol)

        CH<sub>3</sub>CH<sub>2</sub>Br(l) →   ………………
A

elimination to form CH2CH2 (ethene)

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15
Q

Deduce the reaction type from the reagent, then deduce the product.

(LiAlH4 in dry ether, then add dilute HCl(aq))

        CH<sub>3</sub>COOH(l) →   ………………
A

reduction to CH3CH2OH (ethanol)

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16
Q

Deduce the reaction type from the reagent, then deduce the product.

(K2Cr2O7(aq) with H2SO4(aq), heat under reflux)

CH<sub>3</sub>CH<sub>2</sub>OH<sub>(l)</sub> →   ………………
A

oxidation to CH3COOH (ethanoic acid)

17
Q

CH3CH3CN → CH3CH2COOH

A

reflux with HCl