Topic 10 Flashcards

1
Q

What are the two types of bond fission?

A

Heterolytic and homolytic

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2
Q

What is homolytic bond fission?

A
  • A covalent bond between two atoms breaks and each atom takes an electron
  • formation of free radicals
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3
Q

What is heterolytic bond fission?

A

When a covalent bond is broken between two atoms in a molecule with one taking both electrons

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4
Q

What is produced in complete combustion reactions?

A

CO2+H20

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5
Q

Why do alkanes make good fuels?

A

Release large amounts of heat

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6
Q

What are the products of incomplete combustion?

A

C or CO

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7
Q

Why are alkenes reactive?

A

They have a carbon carbon double bond

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8
Q

What reaction do alkenes undergo?

A

Electrophillic addition

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9
Q

Hydrogenation

A

Alkene+ H2= Alkane
Reagant= Ni
Conditions = high temperature and pressure

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10
Q

Halogenation ( with halogen)

A

Alkene+ Haolgen= Dihaloalkane

C2H4+Br2=CH2BrCH2Br

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11
Q

Halogenation ( with hydrogen halides)

A

Alkene+ Hydrogen halide = halogenoalkanes
Reagant= The hydrogen halide
C2H4+HBr= CH3CH2Br OR CH2BrCH3

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12
Q

Hydration

A

Alkene+ H20 = Alcohol
Reagant = H2SO4
Conditions = H20 as steam

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13
Q

What do unsymmetrical alkenes have?

A

More than one end product

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14
Q

Oxidation of primary alcohols

A

-Partial oxidation = aldehyde ( CHO)
Condition = heat under distillation
Reagant= Acidified potassium dichromate
Colour change = Orange - Green

-Further oxidation = carboxylic acid( COOH)
Condition= Heat under reflux
Reagant= Acidified potassium dichromate
Colour change = Orange - Green

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15
Q

Oxidation of secondary alcohols

A

Complete oxidation = ketones ( C-CO-C)
Reagant= Acidified potassium dichromate
Colour change = Orange - Green
Condition = Heat under reflux

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16
Q

Oxidation of tertiary alcohols

17
Q

What reaction does halogenoalkanes undergo?

A
  • Nucleophilic substitution

- SN1 and SN2

18
Q

What are nucleophiles?

A

Have lone pairs of electrons to donate and are attracted to regions of positive charge

19
Q

What reaction do alkanes undergo?

A

Free radical substitution and as they have low reactivity

20
Q

Why are alkanes unreactive?

A
  • carbon to carbon single bond
  • the C and H bonds are non polar
  • The C-C and C-H bonds are relatively strong
21
Q

Free radical substitution for methane and Cl

A
-Alkanes + haolgen = Dihaloalkane or halogenoalkane
Initiation
Cl2 -- Cl. + Cl.
Propagation
CH4+Cl. = CH3. + HCl
CH3.+ Cl2 = CH3Cl+ Cl.
Termination
Cl.+Cl.= Cl2
CH3.+CH3. = C2H6
CH3.+ Cl. = CH3Cl
22
Q

What is the test for unsaturation?

A
  • When bromine water is added to an alkene and the water is decolourised because there is a double bond
  • When added to an alkane there is no colour change
  • Unsaturated = double bond or triple bond
  • Saturated = single bond
23
Q

What is PVC?

A

A polymer made from chloroethene

24
Q

How are additional polymers formed?

A

When smaller unsaturated molecules react together

25
Draw the additional polymer of chloroethane
26
Combustion of alcohols
- Incomplete combustion = CO+ H20 OR C+H20 - Complete combustion = CO2 + H20 - As the number of carbons increase so does the enthalpy change ( becomes more negative)
27
What two functional groups react together to get an Ester and water?
Carboxylic acid + Alcohol
28
Esters
- Reagant = Concentrated sulfuric acid ( H2SO4) | - Nucleophillic substitution reaction
29
Reaction of ethanoic acid and ethanol
30
Draw the structure of benzene
31
What reaction does Benzene undergo?
Electrophillic substitution
32
What is structural isomerism?
Having the same molecular formula but different arrangement of the atoms
33
What three things increase the BP of organic compounds?
- molar mass, functional group and structure
34
Why do branched isomers have a lower BP then straight chained isomers?
The branches prevent the molecules from getting close together which decreases the strength of the london forces
35
What is the physical evidence for benzene structure?
The length and strength of the carbon to carbon bonds are intermediate between the single and double bond
36
What is the chemical evidence for structure of benzene?
Undegos substiturion reactions and not addition reactions