Carboxylic Acids + Derivatives Flashcards

0
Q

Why is alkali catalysis more efficient?

A

Non-reversible as acid formed loses its proton by reacting with excess alkali turning it into a -ve ion which doesn’t react with the alcohol.

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1
Q

What products form when an ester is hydrolysed in the presence of acid and in the presence of alkali?

A

Acid - acid + alcohol

Alkali - salt + alcohol

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2
Q

What are the products of the reaction between a carboxylic acid and PCl5?

A

acyl chloride, POCl3 and HCl. (misty white fumes, dense white smoke with ammonia, turns damp blue litmus red).

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3
Q

Describe Le Chatelier’s Principle.

A

If a DYNAMIC equilibrium is disturbed by changing the conditions, the position of equilibrium moves to counteract the change.

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4
Q

What are the products of the reaction between ethanoyl chloride and water?

A

ethanoic acid and HCl.

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5
Q

what are the products of the reaction between ethanoyl chloride and ethanol?

A

Ethyl ethanoate and HCl.

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6
Q

What are the products of the reaction between ethanoyl chloride and ammonia?

A

Ethanamide and ammonium chloride (HCl immediately reacts with NH3).

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7
Q

What is the equation for the reaction between ethanoyl chloride and ammonia?

A

CH3COCl + 2NH3 (aq) —> CH3CONH2 + NH4Cl

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8
Q

What are the products of the reaction between ethanoyl chloride and methylamine?

A

N-methylethanamide + HCl.

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9
Q

where are the double bonds in a molecule of unsaturated fat?

A

In the hydrocarbon chain of the carboxylic acid.

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10
Q

Give the equation for the reaction of ethanal with a solution of of iodine in aqueous sodium hydroxide.

A

CH3CHO + 3I2 + 4NaOH –> CHI3 + HCOO-Na+ + 3NaI + 3H2O

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11
Q

Give the equation for the oxidation of ethanol to produce ethanoic acid.

A

CH3CH2OH + 2[O] –> CH3CH2COOH + H2O

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12
Q

Give the equation for the hydrolysis of ethylethanoate in ALKALINE conditions.

A

CH3COOCH2CH3 + NaOH –> CH3COO-Na+ + CH3CH2OH

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13
Q

What do trans isomers do?

A

raise level of harmful form of cholesterol in blood –> increased heart disease risk.

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19
Q

Why is it better to use an acyl chloride rather than a carboxylic acid in esterification?

A

It is a stronger electrophile as the C delta + is STRONGER as Cl is more electronegative than the O in the OH group.

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