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Chemistry reaction conditions

Total questions: 21

Worksheet time: 16mins

Name
Class
Date
1.

Alkene reaction - Combustion

a)

incomplete - yellow flame(luminous)

b)

complete - blue flame(non-luminous)

c)

no. of carbon ^, soot ^

d)

UV light

2.

Alkene reaction - Substitution

a)

Chlorine, Cl2Cl_2   - pale green to colourless

b)

Bromine, Br2Br_2  - reddish brown change to colourless

c)

Initiation, Propagation, Termination

d)

UV light

3.

Alkene reaction - Cracking

a)

Large alkane --> small alkane, alkene

b)

Thermal

-> 800°C

c)

Catalytic

-> 450°C

-> aluminium (III) oxide mixed with silica / zeolite

d)

UV light

4.

Alkene reaction - Hydrogenation

a)

Hydrogen gas, H2H_2  

b)

Thermal

-> 800°C

c)

Nickel, Ni

d)

140°C - 200°C

5.

Alkene reaction - Halogenation

a)

Halogen in CCl4CCl_4  

b)

Room temperature

c)

Chlorine, Cl2Cl_2   - pale green decolourised

d)

Bromine, Br2Br_2   - reddish brown decolourised

6.

Alkene reaction - Bromine water test (identify presence of C=C double bond)

a)

Bromine water

b)

Room temperature

c)

In the dark

d)

Bromine, Br2Br_2   - reddish brown decolourised

7.

Alkene reaction - Addition of hydrogen halides (symmetrical, unsymmetrical)

a)

Hydrogen halides, HX (HCl, Hbr, HI)

b)

Room temperature

c)

Follows Markovnikov rule (Hydrogen atom added to carbon with greatest number of hydrogen atoms)

d)

In the dark

8.

Alkene reaction - Hydration (addition of steam)

a)

steam in H3PO4H_3PO_4  

b)

300°C

c)

Follows Markovnikov rule (Hydrogen atom added to carbon with greatest number of hydrogen atoms)

d)

70atm

9.

Alkene reaction - Mild oxidation

a)

steam in H3PO4H_3PO_4  

b)

Dilute acidified potassium manganate (VII), KMnO4KMnO_4  

c)

Cold

d)

Purple KMnO4KMnO_4   decoulorised, brown precipitate ( MnO2MnO_2  ) formed

10.

Alkene reaction - Oxidation (oxidative cleavage - unsubstituted, substituted)

a)

Can be used to identify structure of alkene 

b)

Concentrated acidified potassium manganate (VII), KMnO4KMnO_4  

c)

Hot

d)

Purple KMnO4KMnO_4   decoulorised

11.

Alkene reaction - Polymerisation

a)

Monomer

b)

Concentrated acidified potassium manganate (VII), KMnO4KMnO_4  

c)

Hot

d)

Purple KMnO4KMnO_4   decoulorised

12.

Benzene reaction (substitution) - Halogenation

a)

Halogen, X2 (Cl2, Br2)

b)

Presence of anhydrous FeX3 or AlX3 

c)

Room temperature

d)

Purple KMnO4KMnO_4   decoulorised

13.

Benzene reaction (substitution) - Nitration

a)

Concentrated HNO3

b)

Concentrated H2SO4

c)

55°C

d)

Yellow oil formed

14.

Benzene reaction (substitution) - Friedel-Crafts alkylation

a)

halogenoalkene(RX)

b)

Presence of anhydrous AlCl3 or FeCl3

c)

Room temperature

d)

In the dark

e)

Steamy white fumes of HCl formed

15.

Benzene reaction (substitution) - Friedel-Crafts acylation

a)

acyl chloride (RCOCl)

b)

Presence of anhydrous AlCl3 or FeCl3

c)

Reflux on water bath

d)

80°C

e)

Steamy white fumes of HCl formed

16.

Benzene reaction (substitution) - Sulphonation

a)

Fuming H2SO4 (saturated H2SO4 with SO3)

b)

Heat under reflux

c)

Concentrated H2SO4

d)

80°C

e)

Steamy white fumes of HCl formed

17.

Benzene reaction (Addition) - Hydrogenation

a)

Benzene vapour, H2(g)

b)

Finely divided Nickel, Ni

c)

High temperature

d)

High pressure

e)

Steamy white fumes of HCl formed

18.

Alkylbenzene reaction (Side chain) - Halogenation (free radical substitution)

a)

Halogens (Cl2, Br2) in CCl4

b)

Initiation, Propagation, Termination

c)

Chlorine - pale green to colourless

d)

UV light

e)

Bromine - reddish brown to colourless

19.

Alkylbenzene reaction (Side chain) - Oxidation

a)

Acidified KMnO4

b)

Activating - electron donating (ortho-para), Deactivating - electron accepting (meta)

c)

Heat under reflux

d)

benzoic acid as product

e)

alkyl group must have a benzylic hydrogen

20.

Alkylbenzene reaction (Benzene ring) - Nitration

a)

Concentrated HNO3

b)

Activating - electron donating (ortho-para), Deactivating - electron accepting (meta)

c)

Heat under reflux

d)

30°C

e)

alkyl group must have a benzylic hydrogen

21.

Alkylbenzene reaction (Benzene ring) - Halogenation

a)

Halogen, X2 (Cl2, Br2)

b)

Activating - electron donating (ortho-para), Deactivating - electron accepting (meta)

c)

Presence of anhydrous FeX3 or AlX3

d)

In the dark

e)

Room temperature