Every AS chemistry chemical reaction, 9701 CIE, organic and inorganic

99 reactions in total, let me know if I missed any.

INORGANIC:

• 2NaOH + Cl2​ -> NaCl + NaClO + H2​O ← for COLD DILUTE NaOH

• 6NaOH + 3Cl2​ -> 5NaCl + NaClO3​ + 3H2​O ← for HOT concentrated NaOH

• Na2O + H2O -> NaOH

• Na2O + 2HCl -> 2NaCl + H2O

• MgO + H2O -> Mg(OH)2

• MgO + 2HCl -> MgCl2 + H2O

• Al2O3 + H2O -> NO REACTION

• Al2O3 + 6HCl -> 2AlCl3 + 3H2O

• Al2O3 + 2NaOH + 3H2O -> 2NaAl(OH)4

• SiO2 + H20 -> NO REACTION

• SiO2 + 2NaOH -> NaSiO3 + H2O ← HOT NaOH

• P4O10 + 6H2O -> 4H3PO4

• P4O10 + 12NaOH -> 4Na3PO4 + 6H2O

• SO2 + H2O -> H2SO3 (sulfurous acid)

• SO2 + 2NaOH -> Na2SO3 + H2O

• NaSO3 + H2O + SO2 -> 2NaHSO3

• CaO + SO2 -> CaSO3

• CaO + SO2 + 2H2O + ½O2 -> CaSO4.2H2O

• CaCO3 + SO2 -> CaSO3 + CO2

• Ca(OH)2 + SO2 -> CaSO3 + H2O

• CaO + ½O2 + SO2 -> CaSO4

• 2Na(s) + Cl2(g) -> 2NaCl(s)

• Mg(s) + Cl2(g) -> MgCl2(s)

• 2Al(s) + 3Cl2(g) -> Al2Cl6(s)

• Si(s) + 2Cl2(g) -> SiCl4(l)

• 2P(s) + 5Cl2(g) -> PCl5(s)

• Al2Cl6 + 12H2O -> 2[Al(H2O)6]3+ + 6Cl-

• SiCl4 + 2H2O -> SiO2 + 4HCl

• PCl5 + 4H2O -> H3PO4 + 5HCl

• 2M(s) + O2 -> 2MO (M = metal)

• Mg(s) + 2H2O -> Mg(OH)2 + H2 (cold)

• Mg(s) + H2O -> MgO + H2 (hot)

• M(s) + 2H2O -> M(OH)2 + H2 ← M = Ca, Sr, Ba

• M(s) + H2SO4 -> MSO4 + H2 ← M = metal

• M(s) + 2H+ -> M2+ + H2 ← M = metal

• MgO + H2O -> Mg(OH)2 ← pH 9

• CaO + H2O -> Ca(OH)2 ← pH 11-13

• MO + H2O -> M(OH)2 ← pH 12-14 – M = Sr, Ba, Ra

• M(s) + H2SO4 -> MSO4 + H2 ← M = metal

• M(s) + 2H+ -> M2+ + H2 ← M = metal

• MO + H2SO4 -> MSO4 + H2O ← M = metal

• MO + 2H+ -> M2+ + H2O ← M = metal

• M(OH)2 + H2SO4 -> MSO4 + 2H2O ← M = metal

• M(OH)2 + 2H+ -> M2+ + 2H2O ← M = metal

• CO2 + H2O + CaCO3 -> Ca(HCO3)2

• Ca(HCO3)2 -> CaCO3 + CO2 + H2O ← thermal decomposition

• MgCO3 + HNO3 -> Mg(NO3)2 + CO2 + H2O

• MgCO3 + 2H+ -> Mg2+ + CO2 + H2O

• CO2 + Ca(OH)2 -> CaCO3 + H2O

• M(NO3)2 -> MO + 2NO2 + ½O2 ← thermal decomposition← M = Mg/Ca/Sr/Ba← brown gas, solid melts

• MCO3 -> MO + CO2

• Cl2 + H2O -> HCl + HOCl

• Br2 + H2O -> HBr + HOBr

• H2 + Cl2 -> 2HCl <- in UV light

• H2 + Br2 -> 2HBr <- heat gently

• H2 + I2 -> 2HI <- heat

• NH3(g) + HCl(g) -> NH4Cl(s)

• NaCl + H2SO4 -> HCl + NaHSO4 ← conc H2SO4

• 2NaCl + H2SO4 -> 2HCl + Na2SO4 ← conc H2SO4

• NaBr + H2SO4 -> HBr + NaHSO4 ← conc H2SO4

• HBr + H2SO4 -> Br2 + SO2 + 2H2O ← bromide=stronger reducing agent

• NaI + H2SO4 -> HI + NaHSO4 ← conc H2SO4

• HI + H2SO4 -> I2 + SO2 + 2H2O ← iodide=stronger reducing agent

• 6HI + H2SO4 -> 3I2 + S + 4H2O

• 8HI + H2SO4 -> 4I2 + H2S + 4H2O

• 2Cl2 + 2H2O -> 4HCl + O2

ORGANIC:

• ALKANE + excess O2 -> CO2 + H2O

  • Type: Complete combustion

• ALKANE + limited O2 -> CO/C + H2O

  • Type: incomplete combustion

• ALKANE + Cl2/Br2 -> HALOGENOALKANE

  • Type: homolytic free radical substitution

  • Condition: UV light

• ALKENE + H2 -> ALKANE

  • Type: electrophilic addition

  • Conditions: 150C + Ni catalyst

• ALKENE + Cl2/Br2 -> DI-HALOGENOALKANE

  • Type: electrophilic addition

  • Conditions: room temp

• ALKENE + HX(g) -> HALOGENOALKANE

  • Type: electrophilic addition

  • Conditions: room temp

• ALKENE + KMnO4/H2SO4 -> DIOL

  • Type: oxidation/redox/addition

  • Conditions: room temp

• ALKENE + STEAM -> alcohol

  • Type: electrophilic addition

  • Conditions: 300C, 60 ATM, H3PO4

• LOTS OF ALKENE -> ADDITION POLYMER

  • Type: Addition polymerisation

  • Conditions: Very high pressure

• HALOGENOALKANE + NaOH(aq) -> ALCOHOL + Na+X-

  • Type: nucleophilic substitution

  • Conditions: NaOH(aq) + heat under reflux

• HALOGENOALKANE + NaOH(ethanolic) -> Alkene

  • Type: elimination

  • Conditions: NaOH(ethanolic) + heat under reflux

• HALOGENOALKANE + conc. NH3 -> AMINE

  • Type: nucleophilic substitution

  • Condition: Ethanolic solution of ammonia + heat in sealed tube/under high pressure

• HALOGENOALKANE + HCN -> NITRILE

  • Type: nucleophilic substitution

  • Condition: KCN dissolved in ethanol + heat under reflux

• PRIMARY ALCOHOL -> ALDEHYDE

  • Type: oxidation/redox

  • Conditions: K2CrO7/H2SO4, distill

• PRIMARY ALCOHOL -> CARBOXYLIC ACID

  • Type: oxidation/redox

  • Conditions: K2Cr2O7/H2SO4 + heat under reflux

• SECONDARY ALCOHOL -> KETONE

  • Type: oxidation/redox

  • Conditions: K2Cr2O7 + heat under reflux

• ALCOHOL -> ALKENE

  • Type: dehydration

  • Conc. H3PO4/AL2O3/H2SO4

• ALDEHYDE -> CARBOXYLIC ACID

  • Type: oxidation/redox

  • Conditions: K2Cr2O7/H2SO4 + heat under reflux

• ALDEHYDE -> PRIMARY ALCOHOL

  • Type: reduction

  • Conditions: LiAlH4 (dry ether) or NaBH4(aq)

• KETONE -> SECONDARY ALCOHOL

  • Type: reduction

  • Conditions: LiAlH4 (dry ether) or NaBH4(aq)

• ALDEHYDE/KETONE -> HYDROXYNITRILE

  • Type: nucleophilic substitution

  • Conditions: KCN + H2SO4 + heat under reflux

• ALDEHYDE -> CARBOXYLIC ACID with Tollens’ reagent

  • Type: redox

  • Conditions: AgNO4(aq) + NaOH(aq) then add NH3(aq)

• ALDEHYDE -> CARBOXYLIC ACID with Fehling’s solution

  • Type: redox

  • Conditions: Fehling’s solution

• ALDEHYDE/KETONE -> HYDRAZONE

  • Type: nucleophilic addition-elimination

  • Conditions: 2,4-DNPH

• METHYL KETONE/SECONDARY ALCOHOL, ETHANAL, ETHANOL, PROPAN-2-OL -> iodoform/triiodomethane + sodium carboxylate

  • Type: N/A

  • Conditions: I2(aq) + NaOH(aq)

• NITRILE + Na + ETHANOL -> AMINE

  • Type: reduction

• NITRILE + dilute HCl(aq) -> CARBOXYLIC ACID

  • Type: acid hydrolysis

• NITRILE + dilute NaOH(aq) -> CARBOXYLIC ACID SALT

  • Type: alkaline hydrolysis

• CARBOXYLIC ACID + Na(s) -> CARBOXYLIC ACID SALT

  • Type: redox

  • Conditions: dry conditions

• CARBOXYLIC ACID + BASE -> CARBOXYLIC ACID SALT

  • Type: neutralization

• CARBOXYLIC ACID + METAL CARBONATE -> CARBOXYLIC ACID SALT

  • Type: neutralization

  • Effervescence

• CARBOXYLIC ACID + LiAlH4 -> PRIMARY ALCOHOL

  • Type: reduction

  • Conditions: LiAlH4 should be In dry ether

• CARBOXYLIC ACID + ALCOHOL -> ESTER

  • Type: esterification

  • Conditions: Conc H2SO4 catalyst