organohalides + nucleophilic reactions (s n 1/2, e1/e2/e1cb)
DESCRIPTION
ORGANOHALIDES + Nucleophilic Reactions (S N 1/2, E1/E2/E1cB) . CH21 PS CLASS. Preparation of Organohalides. From ALKENES C=C [just review old lessons] FOR TERTIARY ALCOHOLS, we can simply use H-X (gas) X= Cl,Br in ether, 0°C . Preparation of Organohalides. - PowerPoint PPT PresentationTRANSCRIPT
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ORGANOHALIDES + Nucleophilic Reactions (SN1/2, E1/E2/E1cB)
CH21 PS CLASS
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Preparation of Organohalides
• From ALKENES C=C [just review old lessons]• FOR TERTIARY ALCOHOLS, we can simply use
H-X (gas) X=Cl,Br in ether, 0°C
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Preparation of Organohalides
• FOR TERTIARY ALCOHOLS, we can simply use H-X (gas) X=Cl,Br in ether, 0°C – Follows SN1 so a carbocation is formed, – be careful with rearrangements!
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Preparation of Organohalides
• FOR PRIMARY/SECONDARY ALCOHOLS: SOCl2 / PBr3
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Practice
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Alkyl Fluorides
• Also from ALCOHOLS + • HF / Pryidine • (CH3CH2)2NSF3
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Grignard Reagents
• Reaction of R-X with Mg over ether/THF to form R-Mg-X organometallic compound.
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Grignard Reagents: reduction of R-X
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More samples:
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Nucleophilic Reactions
• R-X, alkyl halides are ELECTROPHILES (positive or electron-poor)
• They react with NUCLEOPHILES/BASES (negative or electron-rich)
• Either substitution – C-C-X becomes C-C-blah + X-
• or elimination reactions– C-C-X becomes C=C + X-
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SUBSTITUTION REACTIONS
• S – substitution: R-X + Nu R-Nu + X- • N – Nucleophilic • 1 or 2 unimolecular or bimolecular rates• INVERSION (change of stereochemistry) CAN
HAPPEN!
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Try this first…
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SN2 BIMOLECULAR
• Bimolecular simply refers to the rate depending on BOTH reactants because of the nature of the mechanism
• Rate = k[RX][Nu]• Rate depends on both because there is
ONE SINGLE COLLISION BETWEEN RX and Nu to form a Nu-R-X transition state
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SN2 BIMOLECULAR
100% INVERSION OF STEREOCHEMISTRY OCCURS!
SUBSTRATE
LEAVING GROUP
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Factors that affect SN2 RXNS:
• STERIC EFFECTS TO INCOMING Nu:– C=C-X (vinylic) and Ar-X (aryl) TOTALL UNREACTIVE
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Factors that affect SN2 RXNS:• THE NUCLEOPHILE
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Factors that affect SN2 RXNS:• THE LEAVING GROUP
should be stable on its own as a free anion• Comparing halides, we go down the column
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Factors that affect SN2 RXNS:
• Alcohols and fluorides usually do not undergo SN2 because OH- and F- aren’t good leaving groups
• This is why we use SOCl2 and PBr3 … THEY CONVERT THE –OH INTO A BETTER LEAVING GROUP
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Factors that affect SN2 RXNS:• Reaction SOLVENT can also affect the reaction.• We prefer POLAR APROTIC SOLVENTS– POLAR but no –OH or –NH in the molecule (no
H2O, NH3, etc…)
• Polar protic solvents form a CAGE around Nu
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Practice
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Practice
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Practice
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Practice
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SN1 UNIMOLECULAR
• Unimolecular: rate depends only on the substrate (mechanism), almost opposite of SN2
• Rate = k[RX]• Rate is only dependent on the slowest step
which is the spontaneous dissociation of your leaving group. (molecules just don’t easily dissociate!)
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SN1 UNIMOLECULAR
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SN1 UNIMOLECULAR
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SN1 UNIMOLECULARSTEREOCHEM IS LOST, A RACEMATE FORM IS MADE, but usually not 50:50
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SN1 UNIMOLECULARSTEREOCHEM IS LOST, A RACEMATE FORM IS MADE, but usually not 50:50
An ION PAIR BLOCKS THE OTHER SIDE!
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Factors that affect SN1 RXNS:
• SUBSTRATE:
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Factors that affect SN1 RXNS:
• LEAVING GROUP:
An –OH in acidic medium can become –OH2+ and leave as H2O which is very favorable
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Factors that affect SN1 RXNS:
• NUCLEOPHILE: no effect, almost at all.
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Factors that affect SN1 RXNS:
• SOLVENT: rates increase if you stabilize carbocation transition state.
• POLAR PROTIC!
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Factors that affect SN1 RXNS:
• SOLVENT: rates increase if you stabilize carbocation transition state.
• POLAR PROTIC!
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PRACTICE
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PRACTICE
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PRACTICE
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PRACTICE
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PRACTICE
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PRACTICE
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PRACTICE
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Elimination Reactions
• More compliated (different mechanisms)• The loss of H-X can lead to a MIXTURE of
alkene products (C-C-X C=C + HX)• But we can predict the most stable/major
poduct• ZAITZEV’S RULE: base-induced eliminations
will form more stable alkene
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E2 elimination• Again, bimolecular so a single collision
between your Base B: and the alkyl halide.
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E2 elimination• Anti-periplanar is favored for transition state
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E2 elimination• Anti-periplanar is favored for transition state
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Practice
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Practice
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Practice
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Practice
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E1 reaction
• Unimolecular, ALSO spontaneously forms carbocation, but then followed by loss of H+ (taken by a base B: and not an attack by Nu:)
• COMPETES WITH SN1 reactions!
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E1 reaction
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E1 reactions
• No need for anti periplanar geometry
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PRACTICE
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PRACTICE
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E1cB
• Unimolecular, but this time CARBANION formed because a proton H+ is first removed by a base.
• cB stands for “conjugate base” because you deprotonate your carbon C-H into a C- and H+
• Usually favored for poor leaving groups (e.g. –OH)
• Carbanion can be stabilized with C=O groups nearby
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E1cB
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E1cB
PRESENCE OF C=O NEARBY CAN GIVE RESONANCE STABILIZATION!
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PREDICTING WHAT PREDOMINATES:
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Slight Clarifications: BASE vs. NUCLEOPHILE
BASE• Affinity for a PROTON• Strong base like R-O- or OH-
NUCLEOPHILE• Usually a LEWIS BASE• In this context, how
attracted to a CARBON
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PRACTICE
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PRACTICE
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PRACTICE
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PRACTICE
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PRACTICE
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PRACTICE
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PRACTICE
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PRACTICE
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PRACTICE
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PRACTICE