Organic Chemistry Flashcards

1
Q

Alkanes general formula

A

CnH2n+2

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2
Q

Homologous series

A

Members follow a general formula and react in a similar way increase in boiling point and chain length

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3
Q

What are isomers

A

Same molecular formula but a different arrangement of atoms whithin the molecule

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4
Q

Structural isomers

A

Different structural arrangement of atoms they can be straight chains or branched chains but will ave same molecular formula

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5
Q

Position isomers

A

Functional group of the molecule in a diffferent position of the carbon chain

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6
Q

Syeroisomerism

A

E-z isomerism
Different spatial arrangement
Limited roatation around a double carbon bond

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7
Q

E isomerism

A

Groups apart

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8
Q

Z isomerism

A

Groups together on same side of double bond

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9
Q

Cip priority rules

A

Group on each side of the double bond with higher ar or mr is given higher priority

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10
Q

Fractional distillation of crude oil

A

1)mixture vspouirsed and fed into fractioning column
2)hit bottom cool top
3)vapour rise and condense at different points
4)longer condone at bottom
5)shorter condensed at top
6)prodcucts siphoned off for different uses

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11
Q

Order of substances in fractioning column

A

1)refisru gas
2)petrol
3)naptha
4)kerosene
5)diesel
6)fuel oil
7)bituemen

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12
Q

Long carbon chain

A

Viscous
High bp
Not flammable
Condense and collected at bottom of column

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13
Q

Short carbon chains

A

Low bp
Flammable
Less viscous
Lower boiling point
Rise higher up collected top

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14
Q

Cracking

A

Broken down into small useful molecules

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15
Q

Thermal cracking

A

ProduCe high proportion of alkanes and Alkenes
1200 k temp
7000kpa pressure

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16
Q

Catalytic cracking

A

Produces aromatic compounds
Lower temps normal pressure
Zeolite catalyst

17
Q

Complete combustion of alkanes

A

Relseasw lots of energy
Ch4+2o2 >co2+2h2o

18
Q

Incomplete combustion of alkanes

A

2ch4+3o2>2co +4h2o

19
Q

Catalytic converters

A

Remove carbon monoxide and oxides of nitrogen from alkanes combustion removed from systems
Uses a rhodium catalyst to convert harmful products into more stable products such as co2 or h2o

20
Q

Carbon particulates

A

Incomplete combustion
Small fragments uhnburnt hydrocarbons
Respiratory problems as they polite the air

21
Q

Nucelophile exsmplws

A

Cn:-
:nh3
-:oh

22
Q

Ozone depletion

A

Absorbs uv radiation
Cfcs also do this
Break down carbon-halogen bonds to form free radicals then catalyse ozone depletion

23
Q

Cfc free solvents

A

Prevent them entering atmosphere
Minimises ozone depletion and global warming

24
Q

Nuelcoplhilic substitution

A

Used to produce alcohols or amines from halogenoalkanes

25
Q

Greater mr

A

Lower bond enthalpy broken more Emily rate of reaction of halogenoalkanes is faster

26
Q

Elimination

A

When halogenoalkanes heated to high temps under alcoholic conditions
Nucleopjile acts as a base and accepts a proton
Removed hydrogen
Emilimation of halide producing carbin - carbon double bind an Alkene

27
Q

Bromine water alkene

A

Orange to colourless if double bind preeent

28
Q

Examples of electrophilew

A

Hbr
Br2
H2so4

29
Q

Conditions to form branched chains

A

High pressures and temperatures weak intermolecular forces

30
Q

Uses of polymers

A

Plastic products
Shopping bags -polyethene
Not biodegradable due to being unreactivd bonds

31
Q

PVC

A

Addition polymer waterproof properties

32
Q

Addition polymers

A

Produced from Alkenes where double bond is broken to form repeating unit