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Topic 10

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Total cards: 24•Content version: v4•Public deck•Updated: 8/1/2026

Card preview (24)

#1
Front (Question)

What are the two types of bond fission?

Back (Answer)

Heterolytic and homolytic

#2
Front (Question)

What is homolytic bond fission?

Back (Answer)

• A covalent bond between two atoms breaks and each atom takes an electron • formation of free radicals

#3
Front (Question)

What is heterolytic bond fission?

Back (Answer)

When a covalent bond is broken between two atoms in a molecule with one taking both electrons

#4
Front (Question)

What is produced in complete combustion reactions?

Back (Answer)

CO2+H20

#5
Front (Question)

Why do alkanes make good fuels?

Back (Answer)

Release large amounts of heat

#6
Front (Question)

What are the products of incomplete combustion?

Back (Answer)

C or CO

#7
Front (Question)

Why are alkenes reactive?

Back (Answer)

They have a carbon carbon double bond

#8
Front (Question)

What reaction do alkenes undergo?

Back (Answer)

Electrophillic addition

#9
Front (Question)

Hydrogenation

Back (Answer)

Alkene+ H2= Alkane Reagant= Ni Conditions = high temperature and pressure

#10
Front (Question)

Halogenation ( with halogen)

Back (Answer)

Alkene+ Haolgen= Dihaloalkane C2H4+Br2=CH2BrCH2Br

#11
Front (Question)

Halogenation ( with hydrogen halides)

Back (Answer)

Alkene+ Hydrogen halide = halogenoalkanes Reagant= The hydrogen halide C2H4+HBr= CH3CH2Br OR CH2BrCH3

#12
Front (Question)

Hydration

Back (Answer)

Alkene+ H20 = Alcohol Reagant = H2SO4 Conditions = H20 as steam

#13
Front (Question)

What do unsymmetrical alkenes have?

Back (Answer)

More than one end product

#14
Front (Question)

Oxidation of primary alcohols

Back (Answer)

-Partial oxidation = aldehyde ( CHO) Condition = heat under distillation Reagant= Acidified potassium dichromate Colour change = Orange - Green -Further oxidation = carboxylic acid( COOH) Condition= Heat under reflux Reagant= Acidified potassium dichromate Colour change = Orange - Green

#15
Front (Question)

Oxidation of secondary alcohols

Back (Answer)

Complete oxidation = ketones ( C-CO-C) Reagant= Acidified potassium dichromate Colour change = Orange - Green Condition = Heat under reflux

#16
Front (Question)

Oxidation of tertiary alcohols

Back (Answer)

-NONE

#17
Front (Question)

What reaction does halogenoalkanes undergo?

Back (Answer)

• Nucleophilic substitution - SN1 and SN2

#18
Front (Question)

What are nucleophiles?

Back (Answer)

Have lone pairs of electrons to donate and are attracted to regions of positive charge

#19
Front (Question)

What reaction do alkanes undergo?

Back (Answer)

Free radical substitution and as they have low reactivity

#20
Front (Question)

Why are alkanes unreactive?

Back (Answer)

• carbon to carbon single bond • the C and H bonds are non polar • The C-C and C-H bonds are relatively strong

#21
Front (Question)

Free radical substitution for methane and Cl

Back (Answer)

-Alkanes + haolgen = Dihaloalkane or halogenoalkane Initiation Cl2 -- Cl. + Cl. Propagation CH4+Cl. = CH3. + HCl CH3.+ Cl2 = CH3Cl+ Cl. Termination Cl.+Cl.= Cl2 CH3.+CH3. = C2H6 CH3.+ Cl. = CH3Cl

#22
Front (Question)

What is the test for unsaturation?

Back (Answer)

• When bromine water is added to an alkene and the water is decolourised because there is a double bond • When added to an alkane there is no colour change • Unsaturated = double bond or triple bond • Saturated = single bond

#23
Front (Question)

What is PVC?

Back (Answer)

A polymer made from chloroethene

#24
Front (Question)

How are additional polymers formed?

Back (Answer)

When smaller unsaturated molecules react together