alchohols Flashcards

1
Q

alcohols functional group

A

-OH

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2
Q

how many alky groups does primary alcohol have

A

1

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3
Q

how many alkyl groups do secondary alcohols have

A

2

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4
Q

how many alkyl groups do tertiary alcohols have

A

3

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5
Q

delta on the oxygen

A

oxygen- d+
hydrogen- d-
the OH- bond is polar which means that electrons are pulled together with the electronegative oxygen in the covalent bond

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6
Q

why do alcohols interact with water molecules

A

the d+ charge on the hydrogen bond is attracted to the lone pair of electrons on neighbouring molecules

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7
Q

why are alchols soluble

A

the dipole interaction allows alchols to dissolve in water
but only shorter chain molecules

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8
Q

what effects the solubility

A

the longer the carbon chain the more insoluble it is because the carbons is non polar and reduces the interaction the water can be made with the alcohol

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9
Q

what type of bonding does alcohols have

A

they have hydrogen bonding which is the strongest type of intermolecular force
this means they have higher boiling points then molecules with no hydrogen bonding e.g alkanes
this makes alcohol less volatile

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10
Q

haloalkanes from alcohol

A

reagent alcohol + halide ion
Conditions acid catalyst H2 SO4

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11
Q

Dehydration of alcohol

A

alkenes can be made from the dehydration of alcohol eliminating water
Conditions :acid catalyst, e.g. sulphuric acid or phosphoric acid
ethanol = ethane + water

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12
Q

what are alkanes made for?

A

Polymers for plastic

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13
Q

Elimination reaction

A

Dehydration of non-primary alcohols can lead to 3 different alkenes
The double bond can be formed either side of the carbon that did have the OH group
Make sure you check if it’s E/Z

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14
Q

combustion of alcohols

A

alcohols are a few and can be used to generate energy. They ban quickly and form a light blue flame when burnt. They react with oxygen in the air to form carbon dioxide and water the alcohol is being oxidised.
C2H50H +302 = 2 CO2 +3 H2O

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15
Q

oxidation of alcohol

A

Alcohols can be oxidised to aldehyde ketones and carbonylic acids by as potassium dichloride K2 Cr2 O7
The dichromate will turn from orange Cr2 O7 2- to green chromate ion Cr3+

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17
Q

primary alcohols can be oxidised into?

A

they can be oxidised into aldehydes and then carboxylic acid
to remove the aldehyde from the oxidising agent we use distillation
To to turn it into carboxylic acid we use reflux and excess oxidising agent because it allows for strong heating without losing volatile

18
Q

secondary alcohols can be oxidised into?

A

They can be oxidised into ketones
To turn into a keto use reflux and an oxidising agent

19
Q

tertiary alcohols can be oxidised into?

A

NOTHING because it can only oxidise through burning