Chapter 4- organic reactions Flashcards
1
Q
Nucleophilicity
A
Increases with:
- more negative charge
- less electronegativity
- less steric hindrance
- less protic solvent
2
Q
Nucleophilicity for protic vs aprotic solvents
A
Aprotic: f->Cl-> Br> I
Protic: H helps like a carrier: I> br> Cl> F
3
Q
SN1
A
- 2 steps
- carbocation
4
Q
SN2
A
- 1 step
- stereospecific
- doesn’t occur with tertiary substrates
5
Q
Leaving groups
A
- weak bases
- I- best
- F- worst
6
Q
Redox
A
- Pcc: primary alcohol -> aldehyde