4.1.3- Carboxylic Acids and Esters Flashcards

0
Q

What is the condition for esterification

A

Concentrated sulphuric acid catalyst, reflux

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1
Q

What type of reaction is esterification

A

Condensation

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2
Q

Which way of producing esters has a greater yield

A

Using acid anhydrides as the alternative with carboxylic acids forms a reversible reaction.

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3
Q

What is a hydrolysis reaction

A

Hydrolysis is the breakdown of a compound by reaction with water or hydroxide ions.

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4
Q

What are the conditions for the acid hydrolysis of esters

A

Heat under reflux with dilute H2SO4/HCl

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5
Q

What are the conditions for the alkaline hydrolysis of esters

A

Heat under reflux with aqueous alkali eg. NaOH

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6
Q

Which out of the two methods for hydrolysis of esters forms an irreversible reaction

A

Alkaline hydrolysis

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7
Q

Give 2 uses if esters

A
  1. Perfumes

2. Flavourings

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8
Q

What is a triglyceride

A

A triester of glycerol (propane-1,2,3-triol) and fatty acids

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9
Q

What are fatty acids

A

Long chain carboxylic acids

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10
Q

Why does each number represent in the shorthand notation for fatty acids

A

A:B (x,y…)

A- number of carbon atoms
B- number of double bonds
X,y…- position of double bonds

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11
Q

Which type of unsaturated fatty acid is thought to be bad for health and why

A

Trans-fats, as they behave like saturated fat in the body, they increase low density lipoproteins (LDLs) which transport cholesterol in the blood and also decrease high density lipoproteins (HDLs) which transport cholesterol out of the blood.

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12
Q

Why is increased cholesterol bad for health

A

Bad cholesterol deposits into artery walls, restricting blood flow, leading to increased risk of coronary heart disease/strokes.

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13
Q

Name the process for making biodiesel

A

Transesterification

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14
Q

What is the general reaction for forming biodiesel and the condition.

A

Triglyceride + methanol/ethanol -> biodiesel + glycerol

Conditions: NaOH catalyst

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15
Q

Recap- what is the mechanism and conditions for the formation of alcohols from halogenoalkanes

A

Mechanism- nucleophilic sustitution
Reagent- NaOH
Conditions- reflux