Chapter 20: Amines Flashcards

1
Q

Where can amides be protonated?

A

The oxygen or nitrogen

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2
Q

Why is SN2 of an alkyl halide + ammonium not preferred for amine synthesis?

A

It forms additional di- and try-alkylamine products

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3
Q

What is a good way to make an amine from alkyl halide?

A

SN2 with azide ion (N3-) and then reduction (LiAlH4 or H2/Pd)

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4
Q

What can be used to prepare an amine from a nitro compound?

2 alternatives

A

H2/Pd, heat

or

Metal + acid (Fe, HCl)

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5
Q

What can be used to form an imine from aldehyde or ketone?

A

R-NH2 and H+

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6
Q

What reagent is used to reduce a nitrile to an amine?

A

LiAlH4

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7
Q

How is a diazonium ion formed?

A

An amine is treated with nitrite (NaNO2)

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8
Q

How can a diazonium ion be converted to a halogen?

A

A copper CuX compound (CuBr, CuCl, CuCN..)

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9
Q

What can amines react with to produce an amide?

A

An acyl chloride

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