Alcohol flash cards

1
Q

What are functional groups

A

A group of atoms responsible for the characteristic reactions of a compound

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2
Q

What is the general formula of alcohols

A

CnH(2n+2)O

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3
Q

What is the bond angle around around an oxygen atom in an alcohol

A

104.5

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4
Q

What is the shape and explanation of the bond angle around the oxygen molecule in an alcohol

A

Shape: non linear
bond angle: 104.5
Explanation: 2 bonding pairs and 2 lone pairs

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5
Q

What are aromatic alcohols

A

They have an alcohol group directly attached to the benzene ring e.g phenols

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6
Q

How are alcohols synthesised

A

By hydration of alcohols

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7
Q

Draw hydrogen bonding between an alcohol and water

A

Ensure to label relevant dipoles and hydrogen bonding

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8
Q

How does hydrogen bonding between alcohols affect BP

A

it causes higher boiling point in alcohols that alleges due to strong hydrogen bonds that require more energy to overcome than other forces

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9
Q

What is the trend with solubility of alcohols in water and explanation

A

The bigger the alcohol molecules the less soluble they are in water
Solubility decreases as hydrocarbon chain increases in size due to the OH group has less influence and the solubility of the longer hydrocarbon chain becomes more dominant.

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10
Q

What determines classification of an alcohol

A

The number of carbon atoms directly attached to the carbon atom carrying the -OH group.

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11
Q

What are the reactions of alcohols

A

Combustion
Dehydration
Substitution
Esterification
Oxidation

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12
Q

What do alcohols produce when they undergo combustion

A

They react to form carbon dioxide and water

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13
Q

What is the equation for complete combustion of ethanol

A

C2H6O + 3O2 (arrow) 2CO2 + 3H2O

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14
Q

What is dehydration

A

Removing water from a molecule

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15
Q

What is the dehydrating agent, conditions, product and mechanism for dehydration of alcohols.

A

Dehydrating agent: conc. sulphuric or phosphoric acid
Condition: reflux
Organic product: alkene
Mechanism: Elimination(no need to draw js learn equation)

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16
Q

Elimination mechanism general equation?

A

Alcohol (arrow with reagent on arrow) alkene + waterr

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17
Q

Why can butan-2-ol be dehydrated to form three isomeric alkenes

A

The elimination reaction can produce a double bond between c1 and c2 or c2 and c3
This leads to the formation of two structural isomers of but-1-ene and but-2-ene
But-2-ene exhibits stereoiseomerism because it has 2 different groups attached to each carbon atom so exists as an E/Z isomer

18
Q

How do alcohols form haloalkanes

A

When they react with hydrogen halides

19
Q

How is the hydrogen halide generated

A

An alcohol is heated with sodium halide and dilute sulfuric acid which forms hydrogen halide in situ

20
Q

How is the haloalkane then produced

A

The halogen halide generated in situ reacts with alcohol to produce haloalkane and water

21
Q

General formula for substitution reaction of alcohols?

A

Alcohol + NaX + sulphuric acid -> haloalkane + NaHSO4 + H2O

22
Q

How are esters formed

A

Alcohols reacts with carboxylic acid in the presence of concentrated sulfuric acid to form esters and water (it is a reversible reaction)

23
Q

What type of reaction is esterification

A

Condensation reaction

24
Q

What is condensation reaction

A

This is where two molecules add together with the elimination of water

25
What is the reagent and observations of oxidation of alcohols
Reagent: potassium dichromate (VI) (K2Cr2O7/H+) Observation: when the reagent acts as an oxidising agent it changes from orange to green
26
What can the observation for oxidation of alcohols be used for
Identify when an oxidation has taken place Test tube test for primary,secondary alcohols and aldehydes
27
What is the new bond formed when oxidation occurs
Carbonyl bond (C=O)
28
What is the reagent,condition and equation for the oxidation of primary alcohols into aldehydes
Reagent: acidified potassium dichromate Condition: distillation Equation: alcohol + [O] (arrow) aldehyde + water
29
What is the reagent,condition and equation for further oxidation of aldehydes to carboxylic acid
Reagent: acidified potassium dichromate Condition: reflux and excess reagent Equation: aldehyde + [O] -> carboxylic acid
30
Overall equation for the formation of a carboxylic acid from a primary alcohols due to oxidation.
Alcohol + 2[O] (arrow) carboxylic acid + water
31
What is the reagent, condition and equation for the oxidation of secondary alcohols into ketones
Reagent: acidified potassium dichromate. Condition : reflux Equation: alcohol + [O] (arrow) Ketone + water
32
Why can’t these ketones be oxidised further?
They cannot easily be oxidised further as the C-C bond is too strong
33
Are tertiary alcohols oxidised?
They are not oxidised by potassium dichromate
34
When potassium dichromate (VI) acts as an oxidising agent what does it reduce to
It is reduced to potassium dichromate (III)
35
Draw simple distillation apparatus
Ensure all apparatus are labelled for all marks
36
what is miscibility
where liquids are soluble in other liquids
37
why are alcohols miscible in water
because they can form hydrogen bonds with water molecules
38
how do you show solubility of an alcohol in water
by drawing alcohol and water bonded together by hydrogen bonding including relevant dipoles and labels
39
how can an alkene be synthesised from an alcohol
by elimination
40
how ready are you for alcoholssss
chooseee