Carboxylic Acids and Esters A2 Flashcards

1
Q

What is the functional group for a carboxylic acid

A

COOH

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2
Q

How soluble are carboxylic acids

A

Up to 4 carbons, they are completely soluble in water due to the formation of hydrogen bonds

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3
Q

What are their relativistic melting points

A

They have higher melting points compared to corresponding alkanes due to hydrogen bonds between themselves

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4
Q

What is the functional group for esters

A

COO

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5
Q

How to name esters

A

The first part of the name (methyl) is the number of carbons connected to the O. The second part (methanoate) is the number of carbon atoms connected to the C (this carbon is included)

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6
Q

How to show carboxylic acids are weak acids

A

RCOOH RCOO- + H+

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7
Q

How do carboxylic acids react with bases

A

With hydroxides, a salt and water is produced. With carbonates, a salt with water and CO2 is formed.

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8
Q

How are esters formed

A

Carboxylic acids react with alcohols with a strong acid catalyst

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9
Q

What is formed when esters are hydrolysed

A

Esters react with water with a strong acid/alkali catalyst to form a carboxylic acid and alcohol

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10
Q

What are some uses of esters

A

solvents, plasticisers,

perfumes and food flavourings

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11
Q

What is the alcohol found in vegetable oils and animal fats

A

propane-1,2,3-triol (glycerol)

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12
Q

What is formed when esters are hydrolysed with NaOH

A

Hydrolysed with an alkaline catalyst produces sodium salts (soap) and glycerol

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13
Q

What is biodiesel

A

A mixture of methyl esters of

long-chain carboxylic acids

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14
Q

How is biodiesel produced

A

Reacting vegetable oils with

methanol in the presence of a catalyst

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