Carboxylic Acids & Esters 6.1.3 Flashcards

1
Q

What is a Carboxyl group?

A

COOH

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2
Q

Are Carboxylic Acids soluble in water?

A

Yes.

Ay they can form H bonds

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3
Q

What affects the solubility of Carboxylic Acids?

A

The length of the chain.
The longer the chain the less soluble.
As a result of the increasing non-polar chain, which cannot interact with water molecules.

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4
Q

What is Esterification?

A

When a Carboxylic acid reacts with an alcohol in the presence of a concentrated H2SO4 which acts as a catalyst.

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5
Q

What is the equation for Esterification?

A

Carboxylic Acid + Alcohol → Ester + Water

RCOOH + rOH → RCOOr + H2O

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6
Q

What are uses of Esters?

A

Perfumes
Flavourings
Essential Oils
Adhesives

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7
Q

How are Esters named?

A

The alcohol is put first with “yl” on the end. Then the name of the acid with “oate” on the end.
eg:
Methanol and Propanoic Acid → Methyl Propanoate

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8
Q

What is a Acid Anhydride?

A

A molecule with the functional group containing a two carbon chains connected by an O, and where each end C has an O double bonded to it.

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9
Q

What is the equation for producing a Ester from an Acid Anhydride?

A

Acid Anhydride + Alcohol → Ester + Carboxylic Acid

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10
Q

What happens to an Ester when Hydrolysed.

A

The Ester heated in the presence of water (or OH-), breaking it to produce a Carboxylic Acid (or Carboxylic salt is NaOH or similar) and an Alcohol.

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11
Q

What does Hydrolysis roughly translate to?

A

Breaking with water

Thus showing that the reaction is breaking a molecule in the presence of water.

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12
Q

What is an Acyl Chloride?

A

AKA Acid Chloride.

RCOCl

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13
Q

What are the reactions of an Acyl Chloride with Nucleophiles?

A

Acyl Chloride + H2O → Carboxylic acid + HCl
Acyl Chloride + ROH → Ester + HCl
Acyl Chloride + 2(NH3) → Primary Amide + NH4Cl
Acyl Chloride + Primary Amide → Secondary Amide + Amide Chloride.

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14
Q

What is the Catalyst and Conditions for Esterification?

A

Warm

H2SO4

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