11. Acyl chlorides Flashcards

1
Q

functional group

A

R-COCL e.g. CH3COCl (double bond O)

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2
Q

why are they very reactive

A

Cl can be substituted for other groups

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3
Q

root and suffix and example

Ch3COCl

A

root - number of Cs
suffix - oyl chloride
ethanoyl chloride

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4
Q

reagents (making an acyl chloride)

A

carboxylic acid and SOCl2

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5
Q

products (making an acyl chloride)

A

R-COCL + SO2 + HCl

acyl chloride + sulfur dioxide + hydrogen chloride gas

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6
Q

equation (formation of acyl chloride)

methanoic acid

A

carboxylic acid + Thionyl chloride -> acyl chloride + sulfur dioxide + hydrogen chloride gas

CH3COOH + SOCl2 -> CH3COCl + SO2 + HCl

methanoic acid + thionoyl chloride -> ethyl propanoyl + sulfur dioxide + hydrogen chloride gas

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7
Q

how to seperate acyl chloride from reaction mixture

A

distillation

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8
Q

products

acyl chloride + alcohol ->

A

ester + HCl

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9
Q

acyl chloride + concentrated ammonia ->

A

primary amide + solid ammonium chloride

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10
Q

equation (acyl chloride + concentrated ammonia)

ethanoyl chloride + concentrated ammonia ->

A

acyl chloride + ammonia -> primary amide + ammonium chloride

CH2COCl + 2NH3 -> CH3CONH2 + NH4Cl

ethanoyl chloride + concentrated ammonia -> ethan amide + ammonium chloride

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11
Q

equation (acyl chloride + alcohol)

ethyl chloride + methanol->

A

acyl chloride + alcohol -> ester + hydrogen chloride

CH3COCl + CH3OH -> CH3COOCH3 + HCL

methanoyl chloride + methanol -> ethyl methanoate +

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12
Q

Acyl Chloride + primary amide->
equation
CH3COCl + CH3CH2NH2 ->

A

secondary amide + HCl

CH3CONHCH2CH3 + HCl

butan amide + hydrogen chloride

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