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Posted on Sep 03, 2012 by DJ Kim 0 Comments
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HYDROGENATION
Alkene + Hydrogen Alkane
E.g. C2H4(g) + H2(g) C2H6(g)
Catalyst is Pt(s)
BROMINATION
Alkene + Bromine Vicinal dibromide
E.g. C2H4(g) + Br2(g) CH2BrCH2Br(g)
CHLORINATION
Alkene + Chlorine Vicinal dichloride
E.g. C2H4(g) + H2(g) CH2ClCH2Cl(g)
HYDROHALOGENATION
Alkene + HX Alkyl halide
E.g. C2H4(g) + HBr(g) CH3CH2Br(g)
SUBSTITUTION WITH BROMINE
Alkene + Bromine Organobromine compound + Hydrogen bromide
E.g. C2H6(g) +Br2(l) C2H5Br(l) +HBr(g)
NOTE: This reaction requires the presence of UV light.
HYDRATION
Alkene + Water Alkanol
E.g. C2H4(g) + H2O(g) CH3CH2OH(g)
DEHYDRATION
Alkanol Alkene + Water
E.g. CH3CH2OH(g) C2H4(g) + H2O(g)
FERMENTATION OF GLUCOSE
Aqueous Glucose Ethanol + Carbon Dioxide Gas
I.e. C6H12O6(aq) 2CH3CH2OH(aq) + 2CO2(g)
yeast)
ALPHA DECAY
BETA DECAY
NEUTRALISATION
Acid + Base Salt + Liquid Water
E.g. HCl(aq) + NaOH(aq) NaCl(aq) + H2O(l)
CARBON DIOXIDE AND WATER
Aqueous carbon dioxide + Liquid water Carbonic Acid
I.e. CO2(aq) + H2O(l) H2CO3(aq)
FORMATION OF SULFUR DIOXIDE
Sulfur + Gaseous oxygen Sulfur Dioxide
I.e. S(s) + O2(g) SO2(g)
FORMATION OF SULFUROUS ACID
Gaseous sulfur dioxide + Liquid water Sulfurous acid
I.e. SO2(g) + H2O(l) H2SO3(aq)
FORMATION OF SULFUR TRIOXIDE
Gaseous sulfur dioxide + Gaseous oxygen Sulfur trioxide
I.e. 2SO2(g) + O2(g) 2SO3(g)
FORMATION OF SULFURIC ACID
Gaseous sulfuric acid + Liquid Water Sulfuric acid
I.e. SO3(g) + H2O(l) H2SO4(aq)
FORMATION OF NITROGEN MONOXIDE
Gaseous oxygen + Gaseous nitrogen Gaseous nitrogen monoxide
I.e. O2(g) + N2(g) 2NO(g)
FORMATION OF NITROGEN DIOXIDE
Gaseous nitrogen monoxide + Gaseous oxygen Gaseous nitrogen dioxide
I.e. 2NO(g) + O2(g) 2NO2(g)
FORMATION OF NITRIC ACID
Gaseous nitrogen dioxide + Liquid water Nitric acid + Gaseous nitrogen monoxide
I.e. 3NO2(g) + H2O(l) 2HNO3(aq) + NO(g)
IONISATION OF AN ACID IN WATER
Acid + Liquid Water Hydronium Ion + Anion
E.g. HCl(aq) + H2O(l) H3O+(aq) + Cl-(aq)
E.g. H2SO4(aq) + H2O(l) H3O+(aq) + HSO4-(aq)
ESTERIFICATION
Ethanoic acid reacts with ethanol in the presence of concentrated sulphuric acid as a
catalyst to produce the ester, ethyl ethanoate. The reaction is slow and reversible. To
reduce the chances of the reverse reaction happening, the ester is distilled off as soon as it
is formed.
Alkanoic acid + Alcohol Alkyl alkanoate + Water
sulfuric acid)
(Catalyst: Concentrated