Alchohols Flashcards

1
Q

General formula of alcohol

A

CnH2n+1OH

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2
Q

What is a primary alcohol

A

The -OH group is attached to a carbon that has 1 other carbon attatched to it

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3
Q

Secondary alcohol

A

The -OH group is attached to a carbon that has 2 other carbons attatched to it

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4
Q

Tertiary alcohol

A

The -OH group is attached to a carbon that has 3 carbons attatched to it

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5
Q

Are alcohols polar

A

Alcohols are generally polar molecules due to the the electronegative hydroxyl group which pulls the electrons in the C-OH bond away from the carbon atom

This means the electronegative oxygen draws electron density away from hydrogen , giving it a slightly positive charge - can attract lone pairs on an oxygen forming H bonds

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6
Q

Alcohol + water - smaller vs larger alcohols

A

When you mix an alcohol with water, hydrogen bonds form between the oh- and h20

smaller - completely soluble

Larger - most of the molecule is non polar carbon chain, so there’s less attraction for the polar h20 molecules - less soluble in water

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7
Q

Why do alcohols have low volatility ( don’t easily evaporate into a gas)

A

Alcohols form H bonding with EACH THER

HYdrogen bonding is the strongest type of intermolecular force, so it gives alcohols LOW volatility

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8
Q

ALchohols vs alkanes

A

Alkanes have non polar bonds because electronegativity of C and H is too similar

Intermolecular forces = weak London forces

High volatility = low BP, not much energy required to break London dispersion
Non polar too- can’t form H bonds with each other

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9
Q

Reactions of alcohols

A

Combustion
Oxidation
Dehydrating
Forming halo alkanes

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10
Q

Combustion of alcohols

A

Burn completely in O2 (plentiful supply) to form h20 and co2
EXOTHERMIC reaction , releasing a lot of energy
As the number of C atoms in the chain increases, the au titis of heat released per mole also increases
C-C and C-H bonds broken

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11
Q

Oxidation of primary alcohols

A

Partial oxidation
ALDEHYDE
Potassium dichromate solution+dilute sulphuric acid
Distil out aldehyde once formed

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12
Q

Colour change ? Oxidation for primary alcohol.s

A

Dichromate changes colour from Orange to green ( Cr3+)

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13
Q

Full oxidation of primary alcohols

A

CARBOXYLIC acid

Heat under reflux

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14
Q

Secondary alcohol oxidation

A

Refluxing a secondary alcohol with acidified dichromate will reduce a KETONE and water

Again orange to green

alchohol + [o]—- ketone and water

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15
Q

Tertiary alcohol oxidation

A

DO NOT react with dichromate - solution stays orange
Cannot be oxidised
No hydrogen atom bonded to carbon with OH group for the oxygen to remove

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16
Q

Dehydrating alcohols

A

ALKENES
Eliminate H20
Eliminatin reaction
Alcohol mixed with acid catalyst e.g. H2so4, then heated
Water bonded to carbon atom adjacent to hyxxul carbon

17
Q

Halo alkanes from alcohols

A
HYDROGEN HALIDES 
Heat under reflux 
Sulphuric aci and halide ions 
Hydroxyl group replaced by halide 
Neucleophlic substitution