DJA 5). Alkenes Flashcards

1
Q

general formula of alkenes

A

CnH2n

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2
Q

whats special about alkenes

A

c=c (carbon-carbon double bond)

restricts rotation of groups attached (therefore E/Z isomers)

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3
Q

how many electrons does the c=c contain and what do we think of it as

A

4 electrons
electron dense
so has potential to attract d+ or positive ions
so is reactive

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4
Q

electrophiles are

A

species looking for a pair of electrons (eg H+)

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5
Q

induced dipole of Br2 by c=c

A

electron dense c=c ‘pushes’ electron density in Br2 from one side to another causing a temporary dipole

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6
Q

structure of the carbocation

A

positively charged ion. when the reaction is occurring the Br can attach onto carbon 1,2,3…..

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7
Q

primary secondary and tertiary structures

- how to identify

A

find the special bit (in our case the positive charge)
find the carbon it is related to
find how many carbons this carbon is attached to (1=primary, 2=secondary…)

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8
Q

primary secondary and tertiary structures

- which is least stable

A

primary

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9
Q

primary secondary and tertiary structures

- which is most stable

A

tertiary

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10
Q

electrophilic addition of H2SO4 to alkenes

  • type of reaction
  • what type of h2so4 is used
  • what can happen to the product
A
  • very exothermic
  • conc h2so4 is used
  • product can be converted into alcohol by addition of water (H2SO4 is reformed so has acted as a catalyst
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11
Q

test for c=c

A

add orange Br2 water –> decolourises

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12
Q

polymer defintion

A

large molecule made up of lots of repeating units called monomers

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13
Q

how to modify plastics

A

add plasticisers
they are small molecules that can get in between the chain of polymer, force them apart and allow them to slide over each other

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14
Q

poly(chloroethane) is also known as…

A

PVC

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15
Q

two types of poly(ethene)

A

LOPE

HOPE

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16
Q

when do you get LOPE poly(ethene)

A
high pressure
high temperature
produces branch chain polymers which don't pack well
molecules are flexible
uses - plastic bags, electric cables
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17
Q

when do you get HOPE poly(ethene)

A

just over room temp and pressure
less branching so more closely packed
molecules are inflexible
uses - crates, bottles, buckets

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18
Q

environmental issues with poly(ethene)

A

made from crude oil thereofre non-renewable
inert as non-polar
non biodegradable
high melting point as strong vdw between molecules

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19
Q

alcohol functional group

A

O-H

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20
Q

two ways to produce ethanol

A

direct hydration

fermentation

21
Q

comparing direct hydration and fermentation

- rate of reaction

A

DH vs fermentation

fast vs slow

22
Q

comparing direct hydration and fermentation

- cost

A

DH vs fermentation

expensive vs cheap

23
Q

comparing direct hydration and fermentation

- manpower

A

DH vs fermentation

low vs high

24
Q

comparing direct hydration and fermentation

- purity

A

DH vs fermentation

pure vs impure

25
comparing direct hydration and fermentation | - type of process
DH vs fermentation | continuous vs batch
26
comparing direct hydration and fermentation | - environmental impact
DH vs fermentation | non-renewable (ethene from crude oil) vs renewable (sugar cane)
27
direct hydration equation
h2c=ch2 + H2o --------> h3c-ch2-o-h | H3PO4
28
type of mechanism to make alcohol
electrophilic addition | see hard copy cards
29
fermentation equation
c6h12o6 ------> 2c2h5oh +2co2
30
conditions for fermentation
yeast zymase 35 degrees absence of air
31
what alcohol content does fermentation produce and why
up to 15%, because any greater and yeast is killed
32
what can fermentation alcohol be used for (other than to drink)
biofuel = renewable
33
why are biofuels considered carbon neutral | plus equations
a carbon neutral substance takes in as much CO2 as it produces +6 6CO2 + 6H2O ---> C6H12O6 + 6O2 (photosynthesis) +4 C6H12O6 -----> 2C2H5OH +2CO2 (fermentation) +0 2x C2H5OH + 3O2 ---> 2CO2 + 3H2O (fuel is burnt)
34
why is considering biofuels as carbon neutral too simplistic
co2 will be released at many other points extraction of glucose fermentation (must heat to 35) transporting raw materials
35
oxidation of alcohols | - oxidising agent (what happens to the oxidising agent and what can we see)
``` K2Cr2O7 /HCl acidified potassium dichromate it gets reduced species that gets reduced.... (K+ is a spectator ion) Cr2O7^2- orange ``` Cr^3+ green
36
primary alcohol is oxidised...
twice
37
primary -->....--->....
primary -->aldehyde--->carboxylic acid
38
secondary --> ...
secondary -->ketone
39
tertiary-->...
not possible | no reaction
40
to make an aldehyde we use which method
distillation
41
to make a carboxylic acid we use which method
reflux
42
why do we use different methods to collect aldehydes and carboxylic acids
carboxylic acid = hydrogen bonding = high bp aldehyde = permanent dipole forces = lower bp so have to re-condense the aldehyde to make a carboxylic acid
43
testing for aldehydes and ketones
tollens reagent aldehyde = silver mirror ketone = NVC
44
testing for alcohols
add a very small piece of sodium | if gently fizzes then alcohol, if violent, water or carboxylic acid
45
another way to test for aldehydes (not tollens reagent)
Fehlings solution (blue) --> brick red precipitate
46
haloalkane test
warm then add silver nitrate white prcipitate - chloroalkane slowest cream precipitate - bromoalkane yellow precipitate - iodoalkane fastest
47
carboxylic acid test
add sodium hydrogencarbonate | bubbles = carboxylic acid
48
catalyst and conditions for dehydration of alcohols
Al2O3 600 degrees c conc H2SO4