Kirill L9+10

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  • Created by: Rscottqub
  • Created on: 22-03-19 15:08
How can we produce alkenes?
elimination of alcohols . Elimination of haloalkanes (ie OH acting as base)
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E2 reaction
elimination 2nd order. rate = k[HA][base] . doesnt involve intermediate.
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E1 reaction
elimination 1st order. rate =k[HA] . involves intermediate .
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process E1
1. Halogen leaves 1st since it is good leaving group --> intermediate. 2. base attacks H on adjacent carbon
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process E2
all that happens in E1, but all at once/ all in 1 step
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Regioselectivity of E1
2 products are formed, in unequal quantities
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Which elimination produces more stable alkenes
E1, produces more substituted alkene `
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E2 prefers what type of derivative
3>2>1 (opposite to SN2)
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secondary derivative will undergo
NOT A MIXTURE OF E1/2 - it is not like SN1/2 - look at product to decide
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Bond length shortest to longest
triple, double, single
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Stability of = highest to lowest
tetrasub , tertiary sub, E- disub, Z- disub, terminal sub, monosub
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other ways to produce alkenes
partial reduction of alkynes using lindlar catalyst- +H2. Reduction alkynes using Na in liquid NH3
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ways to produce alkynes
Double elimination of halogenalkane- must start with disub haloalkane
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Markovmikov rule
if HX is added to alkene, the H will attach to C with fewer alkyl groups, the X will attach to C with the most alkyl groups
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in electrophillic addition reactions major and minor product are always produced
false- only major minor if unsymmetrical alkene was started with
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ways to turn alkene --> alcohol
1. alkene plus water with acid (h3O+) presence 2. addition of borane followed by oxidation
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conditions for boration followed by oxidation
BH3, H20, H2O2 , OH
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1st step
hydroboration- borane is regioselctive - where B attaches is position the OH group will ultimatley end up in . B added to side with less stable carbon
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others steps involved
hydroboration, oxidation, hydrolysis
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electrophillic addition of alkynes produces
di halogenalkane
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boration and oxidation of alkynes produces
aldehyde (not alcohol like alkenes)
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Other cards in this set

Card 2

Front

E2 reaction

Back

elimination 2nd order. rate = k[HA][base] . doesnt involve intermediate.

Card 3

Front

E1 reaction

Back

Preview of the front of card 3

Card 4

Front

process E1

Back

Preview of the front of card 4

Card 5

Front

process E2

Back

Preview of the front of card 5
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