ALL AS LEVEL CIE CHEM REACTIONS

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99 Terms

1

rxn for COLD DILUTE NaOH

2NaOH + Cl2​ -> NaCl + NaClO + H2​O

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2

rxn for HOT concentrated NaOH with chlorine

6NaOH + 3Cl2​ -> 5NaCl + NaClO3​ + 3H2​O

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3

rxn for sodium oxide + water

Na2O + H2O -> NaOH

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4

rxn for sodium oxide + hydrochloric acid

Na2O + 2HCl -> 2NaCl + H2O

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5

rxn for magnesium oxide + water

MgO + H2O -> Mg(OH)2

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6

rxn for magnesium oxide + hydrochloric acid

MgO + 2HCl -> MgCl2 + H2O

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7

rxn for aluminium oxide + water

Al2O3 + H2O -> NO REACTION

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8

rxn for aluminium Oxide + hydrochloric acid

Al2O3 + 6HCl -> 2AlCl3 + 3H2O

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9

rxn for aluminium oxide + sodium hydroxide + water

Al2O3 + 2NaOH + 3H2O -> 2NaAl(OH)4

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10

rxn for silicon dioxide + water

SiO2 + H20 -> NO REACTION

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11

rxn for silicon dioxide + sodium hydroxide

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

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12

rxn for phosphorus oxide + water

P4O10 + 6H2O -> 4H3PO4

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13

rxn for phosphorous oxide + sodium hydroxide

P4O10 + 12NaOH -> 4Na3PO4 + 6H2O

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14

rxn for sulfur dioxide + water

SO2 + H2O -> H2SO3 (sulfurous acid)

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15

rxn for sulfur dioxide + sodium hydroxide

SO2 + 2NaOH -> Na2SO3 + H2O

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16

rxn for sodium sulfite + water + sodium dioxide

NaSO3 + H2O + SO2 -> 2NaHSO3

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17

rxn for calcium oxide + sulfur dioxide

CaO + SO2 -> CaSO3

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18

rxn for formation of hydrated calcium sulfate

CaO + SO2 + 2H2O + ½O2 -> CaSO4.2H2O

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19

rxn for calcium carbonate + sulfur dioxide

CaCO3 + SO2 -> CaSO3 + CO2

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20

rxn for calcium hydroxide + sulfur dioxide

Ca(OH)2 + SO2 -> CaSO3 + H2O

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21

rxn formation of calcium sulfate

CaO + ½O2 + SO2 -> CaSO4

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22

rxn for sodium and chlorine

with state symbols

2Na(s) + Cl2(g) -> 2NaCl(s)

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23

rxn for magnesium + chlorine

with state symbols

Mg(s) + Cl2(g) -> MgCl2(s)

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24

rxn for formation aluminium chloride (dimer)

with state symbols

2Al(s) + 3Cl2(g) -> Al2Cl6(s)

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25

Si(s) + 2Cl2(g) -> SiCl4(l)

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26

2P(s) + 5Cl2(g) -> PCl5(s)

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27

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

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28

SiCl4 + 2H2O -> SiO2 + 4HCl

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29

PCl5 + 4H2O -> H3PO4 + 5HCl

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30

2M(s) + O2 -> 2MO (M = metal)

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31

Mg(s) + 2H2O -> Mg(OH)2 + H2 (cold)

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32

Mg(s) + H2O -> MgO + H2 (hot)

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33

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

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34

M(s) + H2SO4 -> MSO4 + H2 ← M = metal

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35

M(s) + 2H+ -> M2+ + H2 ← M = metal

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36

MgO + H2O -> Mg(OH)2 ← pH 9

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37

CaO + H2O -> Ca(OH)2 ← pH 11-13

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38

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

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39

M(s) + H2SO4 -> MSO4 + H2 ← M = metal

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40

M(s) + 2H+ -> M2+ + H2 ← M = metal

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41

MO + H2SO4 -> MSO4 + H2O ← M = metal

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42

MO + 2H+ -> M2+ + H2O ← M = metal

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43

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

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44

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

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45

CO2 + H2O + CaCO3 -> Ca(HCO3)2

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46

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

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47

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

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48

MgCO3 + 2H+ -> Mg2+ + CO2 + H2O

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49

CO2 + Ca(OH)2 -> CaCO3 + H2O

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50

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

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51

MCO3 -> MO + CO2

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52

Cl2 + H2O -> HCl + HOCl

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53

Br2 + H2O -> HBr + HOBr

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54

H2 + Cl2 -> 2HCl <-- in UV light

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55

H2 + Br2 -> 2HBr <-- heat gently

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56

H2 + I2 -> 2HI <-- heat

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57

NH3(g) + HCl(g) -> NH4Cl(s)

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58

NaCl + H2SO4 -> HCl + NaHSO4 ← conc H2SO4

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59

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

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60

NaBr + H2SO4 -> HBr + NaHSO4 ← conc H2SO4

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61

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

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62

NaI + H2SO4 -> HI + NaHSO4 ← conc H2SO4

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63

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

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64

6HI + H2SO4 -> 3I2 + S + 4H2O

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65

8HI + H2SO4 -> 4I2 + H2S + 4H2O

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66

2Cl2 + 2H2O -> 4HCl + O2

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67

ALKANE + excess O2 -> CO2 + H2O

Type: Complete combustion

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68

ALKANE + limited O2 -> CO/C + H2O

Type: incomplete combustion

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69

ALKANE + Cl2/Br2 -> HALOGENOALKANE

Type: homolytic free radical substitution

Condition: UV light

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70

ALKENE + H2 -> ALKANE

Type: electrophilic addition

Conditions: 150C + Ni catalyst

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71

ALKENE + Cl2/Br2 -> DI-HALOGENOALKANE

Type: electrophilic addition

Conditions: room temp

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72

ALKENE + HX(g) -> HALOGENOALKANE

Type: electrophilic addition

Conditions: room temp

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73

ALKENE + KMnO4/H2SO4 -> DIOL

Type: oxidation/redox/addition

Conditions: room temp

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74

electrophilic addition of steam to an alkene, H2O(g) and H3PO4 catalyst

give conditions

ALKENE + STEAM -> alcohol

Conditions: 300C, 60 ATM, H3PO4

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75

LOTS OF ALKENE -> ADDITION POLYMER

Type: Addition polymerisation

Conditions: Very high pressure

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76

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

Type: nucleophilic substitution

Conditions: NaOH(aq) + heat under reflux

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77

HALOGENOALKANE + NaOH(ethanolic) -> Alkene

Type: elimination

Conditions: NaOH(ethanolic) + heat under reflux

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78

HALOGENOALKANE + conc. NH3 -> AMINE

Type: nucleophilic substitution

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

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79

HALOGENOALKANE + HCN -> NITRILE

Type: nucleophilic substitution

Condition: KCN dissolved in ethanol + heat under reflux

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80

PRIMARY ALCOHOL -> ALDEHYDE

Type: oxidation/redox

Conditions: K2CrO7/H2SO4, distill

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81

PRIMARY ALCOHOL -> CARBOXYLIC ACID

Type: oxidation/redox

Conditions: K2Cr2O7/H2SO4 + heat under reflux

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82

SECONDARY ALCOHOL -> KETONE

Type: oxidation/redox

Conditions: K2Cr2O7 + heat under reflux

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83

ALCOHOL -> ALKENE

Type: dehydration

Conc. H3PO4/AL2O3/H2SO4

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84

ALDEHYDE -> CARBOXYLIC ACID

Type: oxidation/redox

Conditions: K2Cr2O7/H2SO4 + heat under reflux

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85

ALDEHYDE -> PRIMARY ALCOHOL

Type: reduction

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

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86

KETONE -> SECONDARY ALCOHOL

Type: reduction

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

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87

ALDEHYDE/KETONE -> HYDROXYNITRILE

Type: nucleophilic substitution

Conditions: KCN + H2SO4 + heat under reflux

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88

ALDEHYDE -> CARBOXYLIC ACID with Tollens’ reagent

Type: redox

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

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89

rxn for oxidation of aldehyde to carboxylic acid

give type and conditions

ALDEHYDE -> CARBOXYLIC ACID with Fehling’s solution

Type: redox

Conditions: Fehling’s solution

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90

rxn for nucleophilic addition-elimination

ALDEHYDE/KETONE -> HYDRAZONE

Conditions: 2,4-DNPH

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91

rxn for iodoform test

and conditions needed

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

Conditions: I2(aq) + NaOH(aq)

<p>METHYL KETONE/SECONDARY ALCOHOL, ETHANAL, ETHANOL, PROPAN-2-OL -&gt; iodoform/triiodomethane + sodium carboxylate</p><p>Conditions: I2(aq) + NaOH(aq)</p>
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92

rxn for formation of amine

NITRILE + Na + ETHANOL -> AMINE

Type: reduction

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93

rxn for acid hydrolysis of nitrile

NITRILE + dilute HCl(aq) -> CARBOXYLIC ACID

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94

rxn for alkaline hydrolysis of nitrile

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

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95

rxn for carboxylic acid + sodium

give type and conditions

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

Type: redox

Conditions: dry conditions

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96

rxn for carboxylic acid + base
and list the type of reaction

CARBOXYLIC ACID + BASE -> CARBOXYLIC ACID SALT

Type: neutralization

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97

rxn for carboxylic acid + metal carbonate

give type and observation

CARBOXYLIC ACID + METAL CARBONATE -> CARBOXYLIC ACID SALT

Type: neutralization

Effervescence

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98

rxn for formation of primary alcohols

and state the type of reaction and the conditions

CARBOXYLIC ACID + LiAlH4 -> PRIMARY ALCOHOL

Type: reduction

Conditions: LiAlH4 should be In dry ether

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99

rxn for esterification

give conditions as well

CARBOXYLIC ACID + ALCOHOL -> ESTER

Conditions: Conc H2SO4 catalyst

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