Chapter 5, Carbonyl Groups (Aldehydes and Ketones) Flashcards

0
Q

What is the functional group of a ketone?

A

C double bond O in the middle of a carbon chain.

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1
Q

What is the functional group of an aldehyde?

A

C double bond O

H

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2
Q

What observation can be make my adding Tollens to an aldehyde/ketone?

A

No reaction with a ketone

An aldehyde produces a silver mirror precipitate.

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3
Q

What is Tollen’s reagent made from?

What is the process?

A

Ammonia solution is added to silver nitrate.

This is then gently warmed with the aldehyde.

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4
Q

What are the observations using Fehling’s solution with aldehydes/ketones?

A

No reaction with ketone.

Aldehyde goes form blue liquid to red precipitate due to Cu2+ going to Cu2O.

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5
Q

What is a carbonyl group?

A

C=O

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6
Q

Primary alcohols are oxidised to…

A

Aldehydes

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7
Q

Secondary alcohols are oxidised to…

A

Ketones

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8
Q

What reagents/conditions are required for oxidation of primary alcohols?

A

Acidified potassium dichromate and dilute H2SO4

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9
Q

What reagents/conditions are needed for oxidation of secondary alcohols?

A

Acidified potassium dichromate and dilute H2SO4, and heat under reflux.

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10
Q

What is used to reduce carbonyl compounds?

A

Sodium tetraborohydrate

NaBH4

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11
Q

What reagents/conditions are needed to reduce carbonyl compounds?

A

Aqueous ethanol under reflux, followed by dilute H2SO4.

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12
Q

What is an aldehyde reduced to?

A

A primary alcohol.

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13
Q

What is a ketone reduced to?

A

A secondary alcohol.

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14
Q

What reagents is used in nucleophilic addition of carbonyl compounds?

A

NaBH4, followed by H2SO4

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15
Q

What is the nucleophile in nucleophilic addition of carbonyl compounds?

A

Hydride ion, :H-

16
Q

What is the other reagent used in nucleophilic addition of carbonyl compounds?

A

HCN

17
Q

What is this toxic reagent formed from?

A

Dilute acid and excess sodium cyanide.

19
Q

What is the nucleophile of the toxic reagent?

A

:CN-