Organic synthesis Flashcards

1
Q

What reagent is needed to make 1-phenylpropan-1-ol from phenyl-c=o-ch2ch3

A

Nucleophilic addition

H2/Ni or NaBH4

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2
Q

How to make aldehyde into nitrile?

A

Add KCN with dilute acid

Will make 2-hydroxynitrile

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3
Q

Explain why it’s better to prepare primary amines from nitriles rather than from halogenalkanes

A

Halogenalkanes have further reactions of primary amines and make impure products
Nitriles have no further reactions and have a single product

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4
Q

What reagents are needed for acylation (electrophilic substitution of COCH# with benzene?)

A

AlCl3

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5
Q

Alkene –> alkane

A

H2 Ni

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6
Q

Amine –> amide

A

acyl chloride

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7
Q

Nitrile –> amine

A

LiAlH4 or H2/Ni

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8
Q

Halogenalkane –> nitrile

A

KCN in ethanol

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9
Q

Aldehyde –> alcohol

A

Aqueous NaBH4

nucleophilic addition

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10
Q

Aldehyde –> 2-hydroxynitrile

A

HCN

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11
Q

Ketone –> 2-hydroxynitrile

A

KCN in ethanol

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12
Q

Halogenalkane –> alkene

A

KOH

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13
Q

Ketone –> alcohol

A

NaBH4

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13
Q

Ketone –> alcohol

A

NaBH4

Nucleophilic addition

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14
Q

Nitrobenzene –> aminobenzene

A

Sn/ HCl

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15
Q

alkene –> alcohol

A

water in presence of concentrated H3PO4

16
Q

Alcohol –> alkene

A

Concentrated H2SO4

In heat