sn2 – substitution, nucleophilic bimolecularchemistry.bd.psu.edu/justik/chem 210/chem 210...

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CHEM 210 Review of SN1, SN2, E1 and E2 SN2 – Substitution, Nucleophilic Bimolecular One step, concerted reaction where both nucleophile and substrate participate in this rate limiting step (bimolecular) Mechanism: Developmental Problem Set: Show S N 2 products for the following reactions: a. b. c. d. e. f. g. h. i. j. k. NaCl DMSO CH 3 Br NaOH CH 3 CN CH 3 Br KO CH 3 CN CH 3 Br NaCN CH 3 CN CH 3 Br NaCN CH 3 CN CH 3 CH 2 CH 2 I CH 3 CH 2 ONa DMF CH 3 CH 2 CH 2 Br Br NaCl DMSO I NaCl DMSO OTs NaCl DMSO OMs NaCl DMSO Br NaOH CH 3 CN

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Page 1: SN2 – Substitution, Nucleophilic Bimolecularchemistry.bd.psu.edu/justik/CHEM 210/CHEM 210 Sn1Sn2E1E1... · CHEM 210 Review of SN1, SN2, E1 and E2 S N2 – Substitution, Nucleophilic

CHEM210ReviewofSN1,SN2,E1andE2

SN2–Substitution,NucleophilicBimolecularOnestep,concertedreactionwherebothnucleophileandsubstrateparticipateinthisratelimitingstep(bimolecular)

Mechanism:

DevelopmentalProblemSet:ShowSN2productsforthefollowingreactions:

a.

b.

c.

d.

e.

f.

g.

h.

i.

j.

k.

NaClDMSO

CH3Br

NaOHCH3CN

CH3Br

KOCH3CN

CH3Br

NaCNCH3CN

CH3Br

NaCNCH3CN

CH3CH2CH2I

CH3CH2ONaDMF

CH3CH2CH2Br

Br NaClDMSO

I NaClDMSO

OTs NaClDMSO

OMs NaClDMSO

Br NaOHCH3CN

Page 2: SN2 – Substitution, Nucleophilic Bimolecularchemistry.bd.psu.edu/justik/CHEM 210/CHEM 210 Sn1Sn2E1E1... · CHEM 210 Review of SN1, SN2, E1 and E2 S N2 – Substitution, Nucleophilic

l.

m.

n.

o.

p.

q.

r.

s.

t.

u.

v.

w.

x.

Br KOCH3CH3CN

Br LiOCH3CN

Br NaCNCH3CN

BrCH3CN

OK

O

CH3CNCl KCN

CH3CNOK

O

Cl

OTsNaClDMSO

OTsNaClDMSO

BrNaCNDMF

NaSHCH3CNH

Br

NaSHHMPA

H

Cl

KOCH3CN

OBr

KOCH3CN

Br

Page 3: SN2 – Substitution, Nucleophilic Bimolecularchemistry.bd.psu.edu/justik/CHEM 210/CHEM 210 Sn1Sn2E1E1... · CHEM 210 Review of SN1, SN2, E1 and E2 S N2 – Substitution, Nucleophilic

SN1–Substitution,NucleophilicUnimolecularTwostepreactionwhereonlythesubstrateparticipatesinthisratelimitingstep(unimolecular)

Rate=k[R-X]

Mechanism:

DevelopmentalProblemSet:ShowSN1productsonly(evenwhenE1competes)forthefollowingreactions:

a.

b.

c.

d.

e.

f.

g.

h.

i.

BrH2O

BrCH3OH

BrOH

BrOH

O

I OH

NaSH

I OH

NaS

TsO OH

NaCN

H2OCl

OH

OCl

CC X

Nu

Nu C

racemic

Step 1slow

Step 2

or

fastC

X

For nucleophiles of the type H-Nuthere is a third deprotonation stepusually to give H-X

Page 4: SN2 – Substitution, Nucleophilic Bimolecularchemistry.bd.psu.edu/justik/CHEM 210/CHEM 210 Sn1Sn2E1E1... · CHEM 210 Review of SN1, SN2, E1 and E2 S N2 – Substitution, Nucleophilic

j.

k.

l.

m.

n.

o.

p.

q.

r.

s.

t.

u.

NaSHH2O

Br

OH

NaCNOMs

OHBr

Br

OH

OHBr

H2OBr

OK

OBr

H2O

Br

H2ONaCN

H2ONaSHBr

NaCNBr

OH

OHBr ONa

O

OHBr KCN

Page 5: SN2 – Substitution, Nucleophilic Bimolecularchemistry.bd.psu.edu/justik/CHEM 210/CHEM 210 Sn1Sn2E1E1... · CHEM 210 Review of SN1, SN2, E1 and E2 S N2 – Substitution, Nucleophilic

E2–Elimination,BimolecularOnestep,concertedreactionwherebothbaseandsubstrateparticipateinthisratelimitingstep(bimolecular)

Rate=k[B:][R-X]

Mechanism:

DevelopmentalProblemSet:ShowE2productsonlyforthefollowingreactions:

a.

b.

c.

d.

e.

f.

g.

h.

i.

j.

Br

OK

DMSO, Δ

I DMSO, ΔDBN

Br DMF, Δ

tBuOK

Cl DMF, ΔLiOH

OTf CH3CN, ΔCH3OK

CH3CN, ΔCH3OK

Br

CH3CN, ΔDBNBr

Br OK

DMSO, Δ

Cl OK

DMSO, Δ

Cl OK

DMSO, Δ

C

C X XH

B C

C

B H

anit-periplanargeometry

Page 6: SN2 – Substitution, Nucleophilic Bimolecularchemistry.bd.psu.edu/justik/CHEM 210/CHEM 210 Sn1Sn2E1E1... · CHEM 210 Review of SN1, SN2, E1 and E2 S N2 – Substitution, Nucleophilic

k.

l.

m.

n.

o.

p.

q.

r.

s.

t.

u.

v.

Br

DMSO, ΔDBN

Br OK

HMPA, Δ

Br OK

DMSO, Δ

Br OKPh

DBU, Δ

OK

DMSO, Δ

I

DMSO, ΔDBN

Br

DMSO, ΔDBN

I

Br

OK

DBU, Δ

Ph

OTs

DMSO, ΔLDA

Ph

OTs

DMSO, ΔLDA

DMSO, ΔDBN

Br

DMSO, ΔDBN

Br

Page 7: SN2 – Substitution, Nucleophilic Bimolecularchemistry.bd.psu.edu/justik/CHEM 210/CHEM 210 Sn1Sn2E1E1... · CHEM 210 Review of SN1, SN2, E1 and E2 S N2 – Substitution, Nucleophilic

E1–EliminationUnimolecularTwostepreactionwhereonlythesubstrateparticipatesinthisratelimitingstep(unimolecular)

Rate=k[R-X]

Mechanism:

DevelopmentalProblemSet:ShowE1productsonlyforthefollowingreactions:

a.

b.

c.

d.

e.

f.

g.

h.

Br H2O, Δ

I CH3OH, Δ

OMs OH, Δ

OH, Δ

Br

H2O, Δ

Cl

OTs

CH3OH, Δ

OTs

CH3OH, Δ

OTs

CH3OH, Δ

CC X

C

Step 1slow

Step 2

fast

X

H CH

C

CHB

C

CB H

Page 8: SN2 – Substitution, Nucleophilic Bimolecularchemistry.bd.psu.edu/justik/CHEM 210/CHEM 210 Sn1Sn2E1E1... · CHEM 210 Review of SN1, SN2, E1 and E2 S N2 – Substitution, Nucleophilic

i.

j.

k.

l.

m.

n.

o.

p.

q.

r.

s.

t.

u.

v.

Br

OH, Δ

O

H2O, Δ

Br

Br

CH3OH, Δ

I

CH3OH, Δ

BrCH3OH, Δ

Br CH3OH, Δ

OTs

H2O, Δ

CH3OH, Δ

Br

H2O, Δ

Br

Cl

CH3OH, Δ

Br H2O, Δ

I CH3OH, Δ

OMs OH, Δ

OH, Δ

Br

Page 9: SN2 – Substitution, Nucleophilic Bimolecularchemistry.bd.psu.edu/justik/CHEM 210/CHEM 210 Sn1Sn2E1E1... · CHEM 210 Review of SN1, SN2, E1 and E2 S N2 – Substitution, Nucleophilic

KEYSN2a.

CH3Cl

b.

c.

d.

e.

f.

CH3CH2CH2OCH2CH3

g.

h.

i.

j.

k.

l.

m.

NaClDMSO

CH3Br

NaOHCH3CN

CH3Br CH3OH

KOCH3CN

CH3Br H3CO

NaCNCH3CN

CH3Br CH3CN

NaCNCH3CN

CH3CH2CH2I CH3CH2CH2CN

CH3CH2ONaDMF

CH3CH2CH2Br

Br NaClDMSO Cl

I NaClDMSO Cl

OTs NaClDMSO Cl

OMs NaClDMSO Cl

Br NaOHCH3CN

OH

Br KOCH3CH3CN

OCH3

Br LiOCH3CN

O

Page 10: SN2 – Substitution, Nucleophilic Bimolecularchemistry.bd.psu.edu/justik/CHEM 210/CHEM 210 Sn1Sn2E1E1... · CHEM 210 Review of SN1, SN2, E1 and E2 S N2 – Substitution, Nucleophilic

n.

o.

p.

q.

r.

s.

t.

u.

v.

w.

x.

Br NaCNCH3CN

CN

BrCH3CN

OK

OO

O

CH3CNCl KCN

CN

CH3CNOK

O

Cl O

O

OTsNaClDMSO

Cl

OTsNaClDMSO

Cl

BrNaCNDMF

CN

NaSHCH3CNH

Br

H

SH

NaSHHMPA

H

Cl

SH

H

KOCH3CN

OBr O

O

KOCH3CN

Br O

Page 11: SN2 – Substitution, Nucleophilic Bimolecularchemistry.bd.psu.edu/justik/CHEM 210/CHEM 210 Sn1Sn2E1E1... · CHEM 210 Review of SN1, SN2, E1 and E2 S N2 – Substitution, Nucleophilic

KEYSN1a.

b.

c.

d.

e.

f.

g.

h.

i.

j.

k.

l.

m.

BrH2O

HO

BrCH3OH

H3CO

BrOH

O

BrOH

O

O

O

I OH

NaSHHS

I OH

NaSS

TsO OH

NaCNNC

H2OCl OH

OH

OCl O

O

NaSHH2O

Br SH

OH

NaCNOMs CN

OHBr O

Br

OHO

Page 12: SN2 – Substitution, Nucleophilic Bimolecularchemistry.bd.psu.edu/justik/CHEM 210/CHEM 210 Sn1Sn2E1E1... · CHEM 210 Review of SN1, SN2, E1 and E2 S N2 – Substitution, Nucleophilic

n.

o.

p.

q.

r.

s.

t.

u.

OHBr O

H2OBr OH

OK

OBr

H2OO

O

O

O

+

Br

H2ONaCN CN CN

+

H2ONaSHBr SH SH

+

NaCNBr

OH

CN CN+

OHBr ONa

O

+O

O

H

H

O

O

OHBr KCN

+H

CN

CN

H

Page 13: SN2 – Substitution, Nucleophilic Bimolecularchemistry.bd.psu.edu/justik/CHEM 210/CHEM 210 Sn1Sn2E1E1... · CHEM 210 Review of SN1, SN2, E1 and E2 S N2 – Substitution, Nucleophilic

KEYE2a.

b.

c.

d.

e.

f.

g.

h.

i.

j.

k.

l.

m.

Br

OK

DMSO, Δ

I DMSO, ΔDBN

Br DMF, Δ

tBuOK

Cl DMF, ΔLiOH

OTf CH3CN, ΔCH3OK

CH3CN, ΔCH3OK

Br

CH3CN, ΔDBNBr

Br OK

DMSO, Δ

+ +major

Cl OK

DMSO, Δ

+ +major

Cl OK

DMSO, Δ+

major

Br

DMSO, ΔDBN +

major

Br OK

HMPA, Δ

Br OK

DMSO, Δ

Page 14: SN2 – Substitution, Nucleophilic Bimolecularchemistry.bd.psu.edu/justik/CHEM 210/CHEM 210 Sn1Sn2E1E1... · CHEM 210 Review of SN1, SN2, E1 and E2 S N2 – Substitution, Nucleophilic

n.

o.

p.

q.

r.

s.

t.

u.

v.

Br OKPh

DBU, Δ

Ph

+

major

OK

DMSO, Δ

I

DMSO, ΔDBN

Br

DMSO, ΔDBN

I+

major

Br

OK

DBU, Δ

Ph

OTs

DMSO, ΔLDA H

Ph

Ph

OTs

DMSO, ΔLDA H

Ph

DMSO, ΔDBN

Br

DMSO, ΔDBN

Br

Page 15: SN2 – Substitution, Nucleophilic Bimolecularchemistry.bd.psu.edu/justik/CHEM 210/CHEM 210 Sn1Sn2E1E1... · CHEM 210 Review of SN1, SN2, E1 and E2 S N2 – Substitution, Nucleophilic

KEYE1a.

b.

c.

d.

e.

f.

g.

h.

i.

j.

k.

l.

m.

Br H2O, Δ

I CH3OH, Δ

OMs OH, Δ

OH, Δ

Br

H2O, Δ

Cl

OTs

CH3OH, Δ

OTs

CH3OH, Δ

OTs

CH3OH, Δ+ +

major

Br

OH, Δ

O + +major

H2O, Δ

Br+

major

Br

CH3OH, Δ+ +

major

I

CH3OH, Δ+

BrCH3OH, Δ

Page 16: SN2 – Substitution, Nucleophilic Bimolecularchemistry.bd.psu.edu/justik/CHEM 210/CHEM 210 Sn1Sn2E1E1... · CHEM 210 Review of SN1, SN2, E1 and E2 S N2 – Substitution, Nucleophilic

n.

o.

p.

q.

r.

s.

t.

u.

v.

Br CH3OH, Δ+

major

OTs

H2O, Δ

CH3OH, Δ

Br

H2O, Δ

Br + +

major

Cl

CH3OH, Δ

+

major

Br H2O, Δ

I CH3OH, Δ

OMs OH, Δ

OH, Δ

Br