CH2 Flashcards

1
Q

Definition of Carbon compounds

A

Compounds that contain carbon as their constituent element

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2
Q

Definition of Organic Compounds

A

Compounds originating from living things that containing Carbon element bonded covalently with other element

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3
Q

Definition of Inorganic compounds

A

Compounds originating from non-living materials such as oxides of carbon, carbonate compounds and cyanide compounds

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4
Q

Definition of Hydrocarbon

A

Organic compound that contain only Hydrogen and carbon

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5
Q

Definition of Non-Hydrocarbon

A

Organic compounds that contain carbon, hydrogen and other elements

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6
Q

Definition of Saturated Hydrocarbon

A

Hydrocarbons that contain only single bonds between carbon atoms

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7
Q

Definition of Unsaturated Hydrocarbon

A

Hydrocarbons that contains double or triple bonds between Carbon atoms

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8
Q

2 Main sources of Hydrocarbon

A

Petroleum
crude Oil

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9
Q

2 Stages of oil refining

A

Fractional distillation
cracking

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10
Q

Definition of fractional distillation

A

Seperation of fraction of hydrocarbons in petroleum at different temperature according to the size of the Hydrocarbons

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11
Q

Definition of Cracking (of Hydrocarbons)

A

Cracking of long chain Hydrocarbons into smaller molecules at high temperature using catalyst

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12
Q

Characteristics of Homologous series

A

Same General Formula
same functional group
same chemical properties
Consecutive member differ by 1 Carbon atom and 2 Hydrogen Atoms
Physical properties that gradually increase from one member to the next

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13
Q

General formula of Alkane

A

CnH2n+2

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14
Q

General formula of Alkene

A

CnH2n

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15
Q

General formula of Alkyne

A

CnH2n-2

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16
Q

General formula of Alcohol

A

CnH2n+1OH

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17
Q

General formula of Carboxylic Acid

A

CnH2+1COOH

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18
Q

General formula of Ester

A

CmH2m+1COOCnH2n+1

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19
Q

Functional group of alkane

A

Single bond between carbon atoms

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20
Q

Functional group of alkene

A

Double bond between carbon atoms

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21
Q

Functional group of alkyne

A

Triple bond between carbon atoms

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22
Q

Functional group of Alcohol

A

Hydroxyl

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23
Q

Functional group of Carboxylic Acid

A

carboxyl

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24
Q

Functional group of Ester

A

Carboxylate

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25
Solubility of Alkane, Alkene and Alkyne in organic solvent
Soluble
26
Solubility of Alkane, Alkene and Alkyne in water
Insoluble
27
Electrical conductivity of Alkane, Alkene and Alkyne
Cannot conduct electricity in any states
28
Melting & Boiling point of Alkane, Alkene and Alkyne
increase as molecular size increase
29
Density of Alkane, Alkene and Alkyne
Less dense than water
30
Boiling point of alcohol & carboxylic acid
Low Increase with increasing number of carbon atoms per molecule
31
Physical state at room temperature of Carboxylic acid
First 9 exist as liquid
32
Physical state at room temperature of Alcohol
First 11 exist as liquid
33
Solubility of Methanol, Ethanol and Propanol in water
Miscible in water in all proportions
34
Solubility of Methanoic, Ethanoic and Propanoic acid in water
Very soluble
35
Factor that causes Alkanes to be unreactive
Strong C--C and C--H bond Large amount of energy is required to break
36
Products of complete combustion of Alkane
Carbon Dioxide Water
37
Products of incomplete combustion of Alkane
Carbon Monoxide Water OR Carbon Water
38
Products of Substitution reaction between Alkane and Halogens under Sunlight or UV ray
Each Hydrogen atom in Alkane is replaced ONE BY ONE with a Halogen atom
39
2 Chemical reaction of Alkane
Combustion Reaction with halogens
40
Rule of reaction of Alkane and Halogen
Under sunlight//UV ray
41
Product of combustion of Alkene
Carbon Dioxide Water
42
Product of Hydrogenation of alkene
Alkane
43
Product of Halogenation of alkene
2 Halogen atoms is added to the double bond Colour turns colourless
44
Rules of Hydrogenation of alkene
Presence of catalyst 180C temperature
45
Rule of Halogenation of alkene
Room temperature
46
Product of addition of Hydrogen Halide of alkene
Haloalkene (Bromoetehane, Chloropropane)
47
Rules of addition of Hydrogen Halide of alkene
Room temperature
48
Product of Hydration of alkene
Alcohol
49
Rules of Hydration of alkene
Water as steam 300c 60atm Phosphoric acid as catalyst
50
Products of Oxidation with KMnO4 of Alkene
Purple turns colourless 2 Hydroxyl groups are added to double bond
51
7 reaction of Alkene
Complete combustion Hydrogenation halogenation addition with Hydrogen Halide Addition With KMnO4 Hydration addition polymerisation
52
4 Similarities between Alkanes and alkenes
Hydrocarbons Complete combustion produce CO2 and H2O Same Physical properties Number of carbon atoms are the same
53
2 Method of Producing Ethanol
Fermentation of glucose // starch with presence of catalyst Hydration of Ethene with presence of Catalyst
54
Product of Ethanol fermentation
Ethanol carbon dioxide
55
3 Chemical reaction of alcohol
Combustion Oxidation Dehydration
56
Products of complete combustion of Alcohol
Carbon Dioxide Water
57
Product of oxidation of alcohol
Carboxylic acid
58
Products of dehydration of alcohol
Alkene
59
Procedur of dehydration of alcohol
Alcohol vapour is strongly heated by catalyst
60
Characteristics of alkenes produced through dehydration of alcohol
Burn with yellow sooty flame Decolourise bromine water & KMnO4
61
4 Chemical reaction of Carboxylic Acid
With Base with Metal Carbonate with Metal With alcohol
62
Products of reaction between Carboxylic acid and base
Carboxylate salt Water
63
Products of reaction between Carboxylic acid and Metal Carbonate
Carboxylate salt Water Carbon DIoxide
64
Products of reaction between Carboxylic acid and Metal
Carboxylate salt Hydrogen
65
Products of reaction between Carboxylic acid and alcohol
ester water
66
Rule of reaction between Carboxylic acid and alcohol
Presence of H2SO4
67
2 Physical properties of Ester
Sweet & fruity smell Less dense than water
68
Definition of Isomers
Molecules of the same molecular formula but different structural formula
69
Brief procedure of preparing ester
Add glacial Carboxylic acid into pure alcohol Add 5 drops of Sulphuric acid into the test tube Heat the mixture gently until boils