Alcohols, Aldehydes And Ketones Flashcards

1
Q

What type of reaction produces and aldehyde or ketone ?

A

Oxidation Reaction

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2
Q

How can you prevent a carboxylic acids being formed instead of an aldehyde ?

A

Gentle warming and then distilled off to prevent carboxylic acid formation

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3
Q

Test for a carbonyl group (both aldehydes and ketones) and the Observation

A

Add 2,4-DNPH
Orange red ppt formed
It is then recrystallised to purify into the original aldehyde / ketone, identified by specific melting points

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4
Q

What are the 2 test to identify an aldehyde?

A

Tollens Reagent - produces silver mirror
Fehlings Reagent - blue to red ppt

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5
Q

Test to identify alkene and observation

A

Add bromine / bromine water
Orange to colourless

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6
Q

Test for primary and secondary alcohols and observations

A

Acidified potassium dichromate = orange to green
Acidified potassium manganate = purple to colourless

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7
Q

Test for carboxylic acid and observations

A

Add sodium hydrogen carbonate
CO2 bubbles produced

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8
Q

Test for a methylcarbonyl / methyl ketone group and observations

A

Triiodomethane test
Add iodine and sodium hydroxide
Yellow ppt formed from the CHI3 produced and a antiseptic smell

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9
Q

What reagent is used to reduced aldehydes and ketones into their original alcohols ?

A

Sodium tetrahydridoborate, NABH4, in aqueous solution

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10
Q

Describe the Nucleophilic addition of HCN

A

The CN group breaks the C=O bond and attaches itself to the carbon. The oxygen is left with a single bond and a lone pair of electrons. The lone pair of electrons is transferred to the Hydrogen to form an OH group
Hydroxynitirile produced

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11
Q

What reagent reduces a carboxylic acid into primary alcohol?

A

LiAlH4 - lithium tetrahydridoaluminate

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12
Q

What conditions are require to form an alcohol from a Halogenoalkane ?

A

Warm aqueous sodium or potassium hydroxide

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13
Q

What conditions are require to form an alcohol from a Halogenoalkane ?

A

Warm aqueous sodium or potassium hydroxide

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14
Q

Give reactants and conditions required for the formation of a hydroxynitrile from an aldehyde/ketone

A

Potassium or sodium cyanide is added to sulfuric acid to produce hydrogen cyanide
Temperature of 20c

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15
Q

Why is NaBH4 used for the reduction of aldehydes and ketones but not for carboxylic acids ?

A

It isn’t reactive enough to reduce carboxylic acids

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16
Q

What type of organic products is produced in the reaction between alcohols and hydrogen halides?

A

Halogenoalkane

17
Q

What catalyst is required for the reaction of primary / secondary alcohols with hydrogen chloride?

A

Anhydrous zinc chloride

18
Q

Name the type of mechanism between an alcohol and acyl chloride

A

Nucleophilic Addition elimation

19
Q

What are the conditions and catalyst require for an esterification reaction ??

A

The alcohol and carboxylic acid must not heated in the presence of a strong acid catalyst e.g conc sulfuric acid

20
Q

What is the colour change when ferric chloride is added to phenol?

A

Vivid-purple colour

21
Q

What is the test for phenols ?

A

Add aqueous FeCl3 to test for the presence of phenols
Solutions will turn purple, blue, green or red colour depending on the nature of the phenol

22
Q

What is the product formed when a phenol reacts with ethanoyl chloride?

A

Phenyl ethanoate

23
Q

Considering the acidity of phenol, will it react with NaOH and Na2CO3?

A

Reacts with NaOH but doesn’t with Na2CO3, due to it only being weakly acidic

24
Q

Why does phenol generally react more readily than benzene ?

A

Phenol contains a lone pair of electrons on the oxygen atom. This electron pair is delocalised into the ring structure. Increasing the electron density of the ring and therefore more susceptible to electrophilic attack

25
What is the observation when phenol reacts with bromine?
It will decolourise and forms a white precipitate.
26
What is the acidity of phenol?
Phenol has a pH of around 5-6. (Weakly acidic)
27
What is a phenol?
Aromatic alcohol consisting of a benzene ring and an OH alcohol group
28