Alkanes Flashcards

1
Q

Why can carbon form so many compounds

A
  1. can form 4 covalent bonds
  2. can form single, double or triple bonds
  3. can bond to other carbon atoms to form long chains
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2
Q

Definition of aliphatic

A

A compound containing carbon and hydrogen joined together in straight chains, branched chains or non-aromatic rings.

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3
Q

Definition of alicyclic

A

An aliphatic compound arranges in non-aromatic rings with or without side chains

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4
Q

Definition of aromatic

A

A compound containing a benzene ring

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5
Q

Definition of saturated

A

Single carbon-carbon bonds only

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6
Q

Definition of unsaturated

A

The presence of one or more carbon double bond

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7
Q

Definition of homologous series

A

A series of organic compounds having the same functional group but with each successive member differing by CH2.

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8
Q

Definition of a functional group

A

The part of the organic molecule responsible for its chemical reactions.

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9
Q

General formula of alkanes

A

CxH2x+2

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10
Q

Names of alkanes

A
1 carbon- methane
2 carbons- ethane
3 carbons- propane
4 carbons- butane
5 carbons- pentane
6 carbons- hexane
7 carbons- heptane
8 carbons- octane
9 carbons- nonane
10 carbons- decane
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11
Q

Draw cyclopentane using molecular, structural, displayed and skeletal formulas

A

Check page 12 of study pack

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12
Q

Naming alcohols

A

Contain suffix-ol
Always count from end which will give alcohol lowest number
use di, tri as well for more than 1 alcohol

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13
Q

Naming alkanes with side chains

A

methyl group- CH3
ethyl group- CH2CH3
Write at beginning of name e.g 3-methylpropane

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14
Q

Definition of general formula

A

Simplest algebraic formula of a member of a homologous series

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15
Q

Definition of structural formula

A

The minimal detail that shows the arrangement of atoms in a molecule

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16
Q

Definition of displayed formula

A

The relative positioning of atoms and the bonds between them

17
Q

Definition of skeletal formula

A

The simplified organic formula shown by removing hydrogen atoms from alkyl chains leaving just a carbon skeleton and associated functional groups.

18
Q

Structural isomers

A

Are compounds with the same molecular formula but different structural formula

19
Q

Draw structural isomers with formula C4H8

A

Check study pack p 31

20
Q

Definition of stereoisomers

A

Have the same structural formula but a different arrangement of groups in space

21
Q

Definition of chain isomers

A

different arrangement of carbon atoms

22
Q

Definition of functional group isomers

A

different functional group altogether

23
Q

Defintion of positional isomers

A

different positions of functional groups

24
Q

Complete combustion of alkanes equation

A

CxHy + (x+y/4) O2 –> xCO2 + y/2 H2O

25
Incomplete combustion of alkanes equation
1. CO is produced | 2. only C is produced
26
Why is incomplete combustion bad
Carbon monoxide is released which is toxic.
27
State conditions needed for alkanes to react with halogens
UV light
28
Write reaction of bromine with ethane using structural formula
CH3CH3 + Br2 -->CH3CH2Br +HBr
29
Definition of a radical and show the symbol
A radical is a species with an unpaired electron. | The symbol is a dot
30
What is the name of the mechanism in the reaction between methane and bromine
Radical substitution
31
What are the names of the 3 stages involved in the reaction between and alkane and halogen
Initiation, Propagation and termination
32
What happens in the initiation stage
The halogen is broken in to two radicals under the presence of UV light Br2 --> 2Br. The name of this type of bond breaking is homolytic fission
33
Write equations for propagation stages using bromine and methane
Br. + CH4 --> CH3. + HBr | CH3. + Br2 --> CH3Br + Br.
34
Write 3 equations for the termination stage using bromine and methane
2CH3. -->C2H6 2Br. --> Br2 CH3. + Br. -->CH3Br
35
3 limitations of using radical substitution in organic synthesis
1. Further substitution can occur 2. Substitution at different positions on the C chain can occur 3. The C chain may change length (double) It is difficult to synthesis only desired compounds
36
Write general formula for a cycloalkane
CnH2n
37
Define homolytic fission
The breaking of a covalent bond to form two radicals- one electron from each pair goes to each atom