Oxidation Of Alcohols Flashcards

1
Q

What do primary alcohols oxidise to

A

Aldehydes then oxidise further to carboxylic acids

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2
Q

What do secondary alcohols oxidise to

A

Ketones

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3
Q

Do tertiary alcohols oxidise and why

A

They do not as resistant to oxidation due to lack of hydrogen atoms on the carbon atom to which the hydroxyl group is attached, they do not have hydrogen on C-OH carbon but have a C-C bond to break so needs a stronger oxidising agent

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4
Q

What is aldehyde functional group and how to name

A

CHO with double bond between carbon and oxygen at terminal carbon, ends in anal

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5
Q

What is carboxylic acid functional group and how to name

A

COOH anoic acid

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6
Q

What is ketone functional group and how to name

A

C double bonded to O (carbonyl group) on any carbon other than terminal, ends in anone

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7
Q

How to oxidise primary alcohols to form aldehydes

A

Using an oxidising agent eg aqueous solution of acidified potassium dichromate, heat and distill immediately to prevent further oxidation to carboxylic acid

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8
Q

Equation for oxidation of primary alcohols to aldehydes

A

RCH2OH + [O] ——> RCHO(anal) + H2O

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9
Q

Half equation of oxidation of ethanol primary to form aldehyde

A

CH3CH2OH ——> CH3CHO + 2H+ + 2e-

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10
Q

Formula for oxidising agent and its colour change

A

K2Cr2O7 turns from orange to green when reduced

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11
Q

Conditions for full oxidation of primary alcohol to form carboxylic acid

A

-heat under reflux(prevents aldehyde from escaping before fully oxidising) with excess acidified oxidising agent potassium dichromate

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12
Q

Conditions for oxidation of secondary alcohols to form ketones

A

-oxidised by oxidising agent eg aqueous solution of acidified potassium dichromate and heat under reflux to prevent escape of volatile compounds and increase yield

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13
Q

How to distinguish between primary and secondary alcohols

A

-to distinguish between aldehydes and ketones
-using blue Fehling’s reagent and warm, they have Cu2+ ions that form a red-brown precipitate if an aldehyde present but no change with ketone

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14
Q

Conditions for dehydration of alcohols

A

-heat with excess concentrated phosphoric acid

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15
Q

Equation for dehydration of alcohols

A

Alcohol to alkene and steam

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