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WorksheetsChemistry reaction conditions
Total questions: 21
Worksheet time: 16mins
Alkene reaction - Combustion
incomplete - yellow flame(luminous)
complete - blue flame(non-luminous)
no. of carbon ^, soot ^
UV light
Alkene reaction - Substitution
Chlorine, Cl2 - pale green to colourless
Bromine, Br2 - reddish brown change to colourless
Initiation, Propagation, Termination
UV light
Alkene reaction - Cracking
Large alkane --> small alkane, alkene
Thermal
-> 800°C
Catalytic
-> 450°C
-> aluminium (III) oxide mixed with silica / zeolite
UV light
Alkene reaction - Hydrogenation
Hydrogen gas, H2
Thermal
-> 800°C
Nickel, Ni
140°C - 200°C
Alkene reaction - Halogenation
Halogen in CCl4
Room temperature
Chlorine, Cl2 - pale green decolourised
Bromine, Br2 - reddish brown decolourised
Alkene reaction - Bromine water test (identify presence of C=C double bond)
Bromine water
Room temperature
In the dark
Bromine, Br2 - reddish brown decolourised
Alkene reaction - Addition of hydrogen halides (symmetrical, unsymmetrical)
Hydrogen halides, HX (HCl, Hbr, HI)
Room temperature
Follows Markovnikov rule (Hydrogen atom added to carbon with greatest number of hydrogen atoms)
In the dark
Alkene reaction - Hydration (addition of steam)
steam in H3PO4
300°C
Follows Markovnikov rule (Hydrogen atom added to carbon with greatest number of hydrogen atoms)
70atm
Alkene reaction - Mild oxidation
steam in H3PO4
Dilute acidified potassium manganate (VII), KMnO4
Cold
Purple KMnO4 decoulorised, brown precipitate ( MnO2 ) formed
Alkene reaction - Oxidation (oxidative cleavage - unsubstituted, substituted)
Can be used to identify structure of alkene
Concentrated acidified potassium manganate (VII), KMnO4
Hot
Purple KMnO4 decoulorised
Alkene reaction - Polymerisation
Monomer
Concentrated acidified potassium manganate (VII), KMnO4
Hot
Purple KMnO4 decoulorised
Benzene reaction (substitution) - Halogenation
Halogen, X2 (Cl2, Br2)
Presence of anhydrous FeX3 or AlX3
Room temperature
Purple KMnO4 decoulorised
Benzene reaction (substitution) - Nitration
Concentrated HNO3
Concentrated H2SO4
55°C
Yellow oil formed
Benzene reaction (substitution) - Friedel-Crafts alkylation
halogenoalkene(RX)
Presence of anhydrous AlCl3 or FeCl3
Room temperature
In the dark
Steamy white fumes of HCl formed
Benzene reaction (substitution) - Friedel-Crafts acylation
acyl chloride (RCOCl)
Presence of anhydrous AlCl3 or FeCl3
Reflux on water bath
80°C
Steamy white fumes of HCl formed
Benzene reaction (substitution) - Sulphonation
Fuming H2SO4 (saturated H2SO4 with SO3)
Heat under reflux
Concentrated H2SO4
80°C
Steamy white fumes of HCl formed
Benzene reaction (Addition) - Hydrogenation
Benzene vapour, H2(g)
Finely divided Nickel, Ni
High temperature
High pressure
Steamy white fumes of HCl formed
Alkylbenzene reaction (Side chain) - Halogenation (free radical substitution)
Halogens (Cl2, Br2) in CCl4
Initiation, Propagation, Termination
Chlorine - pale green to colourless
UV light
Bromine - reddish brown to colourless
Alkylbenzene reaction (Side chain) - Oxidation
Acidified KMnO4
Activating - electron donating (ortho-para), Deactivating - electron accepting (meta)
Heat under reflux
benzoic acid as product
alkyl group must have a benzylic hydrogen
Alkylbenzene reaction (Benzene ring) - Nitration
Concentrated HNO3
Activating - electron donating (ortho-para), Deactivating - electron accepting (meta)
Heat under reflux
30°C
alkyl group must have a benzylic hydrogen
Alkylbenzene reaction (Benzene ring) - Halogenation
Halogen, X2 (Cl2, Br2)
Activating - electron donating (ortho-para), Deactivating - electron accepting (meta)
Presence of anhydrous FeX3 or AlX3
In the dark
Room temperature
