Chapt. 13 & 14 Ch. 13- Manifest Destiny Ch. 14- North and South.
Organohalides (Ch 14)
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Transcript of Organohalides (Ch 14)
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John E. McMurry
www.cengage.com/chemistry/mcmurry
Chapter 10 Organohalides
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§ An organic compound containing at least one carbon-halogen bond (C-X) § X (F, Cl, Br, I) replaces H
§ Can contain many C-X bonds § Properties and some uses
§ Fire-resistant solvents § Refrigerants § Pharmaceuticals and precursors
What Is an Organohalide?
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§ Reactions involving organohalides are less frequently encountered than other organic compounds, but reactions such as nucleophilic substitutions/eliminations that they undergo will be encountered
§ Alkyl halide chemistry is model for mechanistically similar but more complex reactions
Why this Chapter?
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§ Find longest chain, name it as parent chain § (Contains double or triple bond if present) § Number from end nearest any substituent (alkyl
or halogen)
10.1 Naming Alkyl Halides
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§ Begin at the end nearer the substituent having its name first in the alphabet
Naming if Two Halides or Alkyl Are Equally Distant from Ends of Chain
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§ C-X bond is longer as you go down periodic table § C-X bond is weaker as you go down periodic table § C-X bond is polarized with slight positive charge on
carbon and slight negative charge on halogen
10.2 Structure of Alkyl Halides
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§ Alkyl halide from addition of HCl, HBr, HI to alkenes to give Markovnikov product (see Alkenes chapter)
§ Alkyl dihalide from anti addition of bromine or chlorine
10.3 Preparing Alkyl Halides from Alkenes: Radical Halogenation
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§ Alkane + Cl2 or Br2, heat or light replaces C-H with C-X but gives mixtures § Hard to control § Via free radical mechanism
§ It is usually not a good idea to plan a synthesis that uses this method
Preparing Alkyl Halides from Alkenes: Radical Halogenation
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§ If there is more than one type of hydrogen in an alkane, reactions favor replacing the hydrogen at the most highly substituted carbons (not absolute)
Radical Halogenation of Alkanes
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§ Based on quantitative analysis of reaction products, relative reactivity is estimated
§ Order parallels stability of radicals § Reaction distinction is more selective with bromine than
chlorine
Relative Reactivity
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§ N-bromosuccinimide (NBS) selectively brominates allylic positions
§ Requires light for activation § A source of dilute bromine atoms
10.4 Preparing Alkyl Halides from Alkenes: Allylic Bromination
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§ Allyl radical is delocalized § More stable than typical alkyl radical by 40 kJ/mol (9 kcal/
mol) § Allylic radical is more stable than tertiary alkyl radical
Allylic Stabilization
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§ Three electrons are delocalized over three carbons § Spin density surface shows single electron is dispersed
10.5 Stability of the Allyl Radical: Resonance Revisited
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§ Allylic bromination with NBS creates an allylic bromide § Reaction of an allylic bromide with base produces a
conjugated diene, useful in the synthesis of complex molecules
Use of Allylic Bromination
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§ Reaction of tertiary C-OH with HX is fast and effective § Add HCl or HBr gas into ether solution of tertiary
alcohol § Primary and secondary alcohols react very slowly and
often rearrange, so alternative methods are used
10.6 Preparing Alkyl Halides from Alcohols
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§ Reaction of RX with Mg in ether or THF § Product is RMgX – an organometallic compound (alkyl-metal
bond) § R is alkyl 1°, 2°, 3°, aryl, alkenyl § X = Cl, Br, I
10.7 Reactions of Alkyl Halides: Grignard Reagents
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§ Alkyllithium (RLi) forms from RBr and Li metal § RLi reacts with copper iodide to give lithium dialkylcopper
(Gilman reagents) § Lithium dialkylcopper reagents react with alkyl halides to
give alkanes
10.8 Organometallic Coupling Reactions
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§ Coupling of two organometallic molecules produces larger molecules of defined structure
§ Aryl and vinyl organometallics also effective § Coupling of lithium dialkylcopper molecules proceeds
through trialkylcopper intermediate
Utility of Organometallic Coupling in Synthesis
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§ In organic chemistry, we say that oxidation occurs when a carbon or hydrogen that is connected to a carbon atom in a structure is replaced by oxygen, nitrogen, or halogen § Not defined as loss of electrons by an atom as in
inorganic chemistry § Oxidation is a reaction that results in loss of electron
density at carbon (as more electronegative atoms replace hydrogen or carbon)
§ Oxidation: break C–H (or (C–C) and form C–O, C–N, C–X
10.9 Oxidation and Reduction in Organic Chemistry
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§ Organic reduction is the opposite of oxidation § Results in gain of electron density at carbon (replacement of
electronegative atoms by hydrogen or carbon) § Reduction: form C–H (or C–C) and break C–O, C–N, C–X
Reduction Reactions
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§ Functional groups are associated with specific levels
Oxidation Levels
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How would you carry out the following syntheses?
Let’s Work a Problem
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Answer
The dialkylcopper reagent should be used (di-butylCuLi) that can be added to cyclohexylBr after cyclohexene is treated with HBr.