Acohols and Ethers Flashcards

1
Q

Why do alcohols have considerably higher boiling points than alkanes of similar molecular mass?

A

Because of the polar OH group which allows hydrogen bonds to set up between the molecules. Hy bonds require more thermal energy to break then van der waals

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2
Q

Why can small chain alcohols dissolve in water?

A

Because the energy released when forming hydrogen bonds with water is sufficient to break the hydrogen bonds between the water molecules.

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3
Q

Why do larger chain Alcohols not dissolve in water?

A

Because the large non-polar hydrocarbon part of the molecule masks the polar hydroxyl group.

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4
Q

How are alcohols prepared?

A

Hydration of an alkene with concentrated sulphuric acid.(can’t produce methanol)
Nucleophilic substitution of a monohalogenoalkane.

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5
Q

Name 3 types of reaction an alcohol can undertake

A

With reactive metals to form alkoxides.
Dehydration to form alkenes
Esterification (fast with an acid chloride?)

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6
Q

What is a symmetrical ether?

A

When both R groups are the same.

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7
Q

How do you name ethers?

A

Add oxy to the end of the shorter alkane, then put the larger chains name on the end.

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8
Q

How do ether boiling points compare with alcohol boiling points?

A

Much lower

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9
Q

Why can’t ethers form hydrogen bonds between its molecules?

A

Because the highly electronegative oxygen atom is not directly bonded to a hydrogen atom.

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10
Q

What can ethers make hydrogen bonds with?

A

The H in water

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11
Q

What is the effect of chain length on solubility of ethers?

A

As the chain length increases the solubility decreases

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12
Q

What does the solubility of ethers make them useful for?

A

Extracting organic molecule from aqueous solutions.

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13
Q

Describe the reactivity of ethers

A

Volatile and highly flammable. When exposed to air they slowly form peroxides which are unstable and can be explosive.

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14
Q

Why are ethers used as solvents?

A

They are relatively inert chemically and most organic compounds dissolve in them. Being volatile the solvent is easily removed by distillation.

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15
Q

How are ethers prepared?

A

Refluxing a halogenoalkane with an alkoxide.

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16
Q

What could ethoxyethane be made from?

A

Heating chloroethane with a solution of potassium ethoxide.