Topic 6-organic chemistry Flashcards

1
Q

Stereoisomer

A

-same structural formula
-diff arrangement in space

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1
Q

Fractional distillation

A

-Diff boiling point
-due to diff chain length

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2
Q

Free radical substitution

A

homiletic bond fission, free radicals

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3
Q

Alcohol bp

A

-oh groups form hydrogen bond
-more E needed

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4
Q

Cracking

A

-release short chain alkane and alkene
-demand increased

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5
Q

Isomers

A

-branched chains
-low sa/less point of contact
-weaker London forces so less e needed

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6
Q

catalytic converter

A

2NO+2CO->N2+2CO2

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7
Q

cynide reaction

A

useful as increase carbon chain length

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8
Q

heating

A

-increase reaction rate
-sealed so products don’t escape

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9
Q

Rate of hydrolysis

A

-ethanol as solvent
-silver nitrate
-measure time taken for precipitate
-same temp and volume of halogen

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10
Q

How can small UV result in a big product

A

Radical recycled each time

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11
Q

UV and hydrogen

A

High bond enthalpy for hydrogen so radical not formed as UV not strong enough

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12
Q

Incineration

A

HCl produced
Toxic

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13
Q

Use of ethanol

A

It increases solubility of halogenoalkane/ dissolves haloalkane and water

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14
Q

How are halides present in halogenoalkanes

A

Hydrolysis of halogenoalkane results in heterolytic bond fission

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15
Q

Distillation

A

Not efficient as aldehydes are made due to having lower bp
Aldehydes condense back to further oxidise into carboxylic acid

16
Q

Distillation-improvements

A

-Anti bumping granules to prevent formation of large bubbles + violent boiling by even distribution of heat
-Thermometer should be at the opposite entrance of condenser
-collect over the right bp range (±1 of bp)
-add more ice mixture to cool as sulphuric acid is very EXOTHERMIC
-conical flask should be open
-water in from the bottom
-reflux-prevent loss of volatile substances
-condenser should be OPEN (no stopper) but between condenser and flask should be closed

17
Q

Burning with smoky flame

A

-Incomplete combustion
-less exothermic

18
Q

Differences in energy change

A

delta H is a value with gaseous atoms, but real practicals might not be gaseous

19
Q

Brown vapour in distillation and reflux

A

Bromine as Br oxidised by conc sulphuric acid

20
Q

Fractional distillation

A

-Alkanes have diff bp
-due to diff carbon chain length

21
Q

Side reaction in catalytic converter

A

-Might react with O2
-No might react with Co2

22
Q

Homologous series

A

-Same functional group
-same general formular
-differ by Ch2

23
Q

Bp of alcohol

A

-OH groups form hydrogen bonds
-More E needed

24
Q

Reasons for cracking

A

-Short alkene and alkane
-useful for starting materials (ex-polymers)
-higher in demand

25
Q

Branched chains

A

-lower SA
-weaker London forces

26
Q

Catalytic converting process

A

-absorbtion of gasses into catalytic surface
-weakening of bonds on catalytic surface
-deabsorbtion of products made

27
Q

Nucleophillic substitution

A

End product reacts with a halo radical (ex-chloroethane reacts with cl radical to form dichloroethene and HCl)

28
Q

Uses of polymers

A

-recycle
-incineration to release E
-feedstock for cracking

29
Q

incineration of poly(chloroethene)

A

-HCl produced
-corrosive

30
Q

elimination

A

-ethanolic
-reflux