fuctional group 1 and 2

?
  • Created by: anna888
  • Created on: 18-10-22 17:09
levels of increasing oxidation
alkane-alcohol-aldehyde-carboxillic acid
1 of 10
what is electrophile, general examples?
attracts and accepts e-. neutral/postively charged species with empty orbital to accept e-.
2 of 10
what is nucleophile, general examples?
electron donor, negively charged/lone pair of e-/pi orbitals
3 of 10
describe SN1 mechanism
one molecule in rds. atom/species breaks off. intermidaate carboation.nucleophile attacks
4 of 10
describe SN2 mechanism
two molecules in rds. nucleophile attacks and species breaks off at same time-bond breaks and forms at same time
5 of 10
best structure for SN1? why
tertiary. 1. hyperconjugation-stablisation of carbocation through its groups. 2. planar shape means nucleophile can readily attack
6 of 10
best structure for SN2?
primary/methyl-nucleophile hindered via physical repulion with more groups
7 of 10
what is hyperconjugation?where is it seen in SN2?
stabilisation of compounds/ions through e- of subsituent atoms. stablisation of transition state compound in SN2
8 of 10
differences in SN1 vs SN2 4
1. steric hindernace drives SN1 due to stabiliastion of cation- prevents SN2 2.nucleophile important in SN2 but not SN1. 3.SN1 prefers polar solvents while SN2 prefers less polar solvents
9 of 10
similarity in SN1 and SN2 1
leaving group important in both- ie its bond strength
10 of 10

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Card 2

Front

what is electrophile, general examples?

Back

attracts and accepts e-. neutral/postively charged species with empty orbital to accept e-.

Card 3

Front

what is nucleophile, general examples?

Back

Preview of the front of card 3

Card 4

Front

describe SN1 mechanism

Back

Preview of the front of card 4

Card 5

Front

describe SN2 mechanism

Back

Preview of the front of card 5
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