chapter 26 - compounds containing the carbonyl group Flashcards

1
Q

What is an aldehyde

A

a C=O Group bonded at the end of a carbon chain

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2
Q

What is a Ketone

A

A C=O group In the middle of a carbon chain

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3
Q

What is a carbonyl compound

A

A carbonyl compound Consists of a carbon oxygen double bond.

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4
Q

Physical properties of carbonyl compounds

A

They are strongly polar, that a permanent dipole dipole forces between the molecules. These forces mean that boiling points are higher than those of alkanes.

Shorter chain aldehydes and ketones mix completely with water because hydrogen bonds form between the oxygen of the carbonyl compound and water

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5
Q

The reactivity of carbonyl compounds

A

The carbon oxygen bond in Carbonyl compounds is strong

This is because there is a big difference in electronegativity between the carbon and oxygen making the bonds strongly polar. So nucleophilic reagents can attack to the delta positive carbon. Also since they contain a double bonds, carbonyl compounds are saturated therefore addition reactions as possible.

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6
Q

Reduction of aldehydes and ketones

A

Many reducing agents will reduce both aldehydes and ketones to alcohols. One such reducing agent is sodium tetrahydridoborate(III). NaBH4.

Aldehydes ate reduced to primary alcohols and H plus acts as a nucleophile

Ketones are reduced to secondary alcohol is in a similar way

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7
Q

Physical properties of carboxylic acids

A

The carboxylic acid group can form hydrogen bonds with water molecules. Carboxylic acids up to 4 carbons are completely soluble in water.

They also form hydrogen bonds with each other in the solid-state therefore they have a much higher melting point then the alkanes of similar relative molecular mass.

One way of identifying a carboxylic acid is to measure its melting point and compare it with tables of no melting points. I thiele can be used.

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8
Q

What is an ester

A

an ester Is derived from a carboxylic acid. The hydrogen from the hydroxide group of the acid is replaced by a hydrogen group so the general formula is RCOOR1

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9
Q

What are the uses of esters

A

They are used as vegetable oils and they are also fats from animals

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10
Q

What is the difference between a fat and an oil

A

Fats are solid at room temperature while oils are liquid at room temperature.

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11
Q

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

A

Glycerol has three O-H bonds
It’s readily forms hydrogen bonds and is very soluble in water. It is a very important chemical in many industries and has a really wide range of uses

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12
Q

What are the uses of glycerol

A

It is used extensively in many pharmaceutical and cosmetic preparations because it attracts water, it is used to prevent appointments and creams from drying out.

It is used as a solvent in many medicines and is present in toothpastes

It is used as a solvent in the food industry for example, for food colouring

It is used to plasticise various materials

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13
Q

Tell me about biodiesel

A

One possible solution to the reliance on crude oil as a source of fuel for motor-
vehicles is is biodiesel.

To make biodiesel the oil is reacted with methanol (with a strong alkali as a catalyst) to form a mixture of methyl esters. Which can be used as a fuel in diesel vehicles with the little or no modification

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14
Q

What are the uses of acylation reactions

A

They are cheaper

They are less corrosive

They do not react with water as readily/easily

It is safer, as the byproduct of its reaction is ethanolic acid rather than hydrogen chloride (HCL)

One important use is the production of aspirin

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15
Q

how does Soap work step-by-step

A

1-Soap interacts between oil and water one clothes/skin are washed
2-Carboxylate ion and dissolves in water and the hydrocarbon end dissolves in oil
3-Soap ions arrange themselves around each drop of oil
4-Each droplet is now surrounded by a negative charge
5-The droplets then repel each other
6-each Charge/molecule forms and ionic interaction with delta H on water molecules
7-this Droplet is then carried away by flowing water

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16
Q

what is a soaponification reaction

A

where the ester bond in a triglyceride is broken. forming a glycerol and fatty acid salts. (fatty acid salts have a strong charge separation on one side causing it to be polar. and they have a hydrophobic tail which is non polar).

17
Q

what is the process of soaponification

A

1: when the soap is shaken with water they arrange themselves into micelles. tails are shielded and the polar heads face outwards
2: micelles exist as a colloid in solution ( arrange themselves to be dispersed)
3: micelles can pick up a small molecule of grease in their interiors. the tails dissolve the oil and the droplet is protected from water.
4: the polar heads give the surface a negative charge which helps to repel other micelles and prevents them from clumping.
5: keeps it as small stabilised droplets
6: micelles are washed away with water