6' Alkenes: Structure and Reactivity

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6. Alkenes Structure and Reactivity

• Based on McMurrys Organic Chemistry, 6th edition

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6.2 Degree of Unsaturation

• Relates molecular formula to possible structures
• Degree of unsaturation number of multiple bonds
  or rings
• Formula for saturated a acyclic compound is
  CnH2n2
• Each ring or multiple bond replaces 2 H's

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Example C6H10

• Saturated is C6H14
• Therefore 4 H's are not present
• This has two degrees of unsaturation
• Two double bonds?
• or triple bond?
• or two rings
• or ring and double bond

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Degree of Unsaturation With Other Elements

• Organohalogens (X F, Cl, Br, I)
• Halogen replaces hydrogen
• C4H6Br2 and C4H8 have one degree of unsaturation
• Oxygen atoms - if connected by single bonds
• These don't affect the total count of H's

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If C-N Bonds Are Present

• Nitrogen has three bonds
• So if it connects where H was, it adds a
  connection point
• Subtract one H for equivalent degree of
  unsaturation in hydrocarbon

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Summary - Degree of Unsaturation

• Count pairs of H's below CnH2n2
• Add number of halogens to number of H's (X
  equivalent to H)
• Don't count oxygens (oxygen links H)
• Subtract N's - they have two connections

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6.3 Naming of Alkenes

• Find longest continuous carbon chain for root,
  must include double bond
• Number carbons in chain so that double bond
  carbons have lowest possible numbers
• Rings have cyclo prefix

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Many Alkenes Are Known by Common Names

• Ethylene ethene
• Propylene propene
• Isobutylene 2-methylpropene
• Isoprene 2-methyl-1,3-butadiene

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Rotation of ? Bond Is Prohibitive

• This prevents rotation about a carbon-carbon
  double bond (unlike a carbon-carbon single bond).
• Creates isomers

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6.5 Cis-Trans Isomerism in Alkenes

• The presence of a carbon-carbon double can create
  two possible structures
• cis isomer - two similar groups on same side of
  the double bond
• trans isomer similar groups on opposite sides
• Each carbon must have two different groups for
  these isomers to occur

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Cis, Trans Isomers Require That End Groups Must
Differ in Pairs

• 180rotation superposes
• Bottom pair cannot be superposed without breaking
  CC

X
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6.6 Sequence Rules The E,Z Designation

• Neither compound is clearly cis or trans
• Substituents on C1 are different than those on C2
• We need to define similarity in a precise way
  to distinguish the two stereoisomers
• Cis, trans nomenclature only works for
  disubstituted double bonds

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E,Z Stereochemical Nomenclature

• Priority rules of Cahn, Ingold, and Prelog
• Compare where higher priority group is with
  respect to bond and designate as prefix
• E -entgegen, opposite sides
• Z - zusammen, together on the same side

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Ranking Priorities Cahn-Ingold-Prelog Rules

• Must rank atoms that are connected at comparison
  point
• Higher atomic number gets higher priority
• Br gt Cl gt O gt N gt C gt H

In this case,The higher priority groups are
opposite (E )-2-bromo-2-chloro-propene
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Extended Comparison

• If atomic numbers are the same, compare at next
  connection point at same distance
• Compare until something has higher atomic number
• Do not combine always compare

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Dealing With Multiple Bonds

• Substituent is drawn with connections shown and
  no double or triple bonds
• Added atoms are valued with 0 ligands themselves

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6.7 Alkene Stability

• Cis alkenes are less stable than trans alkenes
• Compare heat given off on hydrogenation ?Ho
• Less stable isomer is higher in energy
• And gives off more heat
• tetrasubstituted gt trisubstituted gt disubstituted
  gt monosusbtituted

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Comparing Stabilities of Alkenes

• Evaluate heat given off when CC is converted to
  C-C
• More stable alkene gives off less heat
• Trans butene generates 5 kJ less heat than
  cis-butene

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Hyperconjugation

• Electrons in neighboring filled ? orbital
  stabilize vacant antibonding ? orbital net
  positive interaction
• Alkyl groups are better than H

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Electrophilic Addition

• Addition of hydrogen bromide to 2-Methyl-propene
• H-Br transfers proton to CC
• Forms carbocation intermediate
• More stable cation forms
• Bromide adds to carbocation

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Energy Diagram for Electrophilic Addition

• Rate determining (slowest) step has highest
  energy transition state
• Independent of direction
• In this case it is the first step in forward
  direction
• rate is not the same as rate constant

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Electrophilic Addition for preparations

• The reaction is successful with HCl and with HI
  as well as HBr
• Note that HI is generated from KI and phosphoric
  acid

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Regioselectivity

• Addition of HCl to 2-methylpropene
• Regiospecific one product forms where two are
  possible
• If both ends have similar substitution, then not
  regiospecific

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Orientation of Electrophilic Addition
Markovnikovs Rule

• In an unsymmetrical alkene, HX reagents can add
  in two different ways, but one way may be
  preferred over the other
• If one orientation predominates, the reaction is
  regioselective (regiospecific)
• Markovnikov observed in the 19th century that in
  the addition of HX to alkene, the H attaches to
  the carbon with the most Hs and X attaches to
  the other end (to the one with the most alkyl
  substituents)
• This is Markovnikovs rule

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Energy of Carbocations and Markovnikovs Rule

• More stable carbocation forms faster
• Tertiary cations and associated transition states
  are more stable than primary cations

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Mechanistic Source of Regiospecificity in
Addition Reactions

• If addition involves a carbocation intermediate
• and there are two possible ways to add
• the route producing the more alkyl substituted
  cationic center is lower in energy
• alkyl groups stabilize carbocation

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6.10 Carbocation Structure and Stability

• Carbocations are planar and the tricoordinate
  carbon is surrounded by only 6 electrons in sp2
  orbitals
• The fourth orbital on carbon is a vacant
  p-orbital
• The stability of the carbocation (measured by
  energy needed to form it from R-X) is increased
  by the presence of alkyl substituents
• Therefore stability of carbocations 3º gt 2º gt 1º
  gt CH3

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The Hammond Postulate

• A transition state should be similar to an
  intermediate that is close in energy
• Sequential states on a reaction path that are
  close in energy are likely to be close in
  structure - G. S. Hammond

In a reaction involving a carbocation, the
transition states look like the intermediate
G
carbocation
Reaction
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Competing Reactions and the Hammond Postulate

• Normal Expectation Faster reaction gives more
  stable intermediate
• Intermediate resembles transition state

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Non-Hammond Behavior

• More stable intermediate from slower reaction
• Conclude transition state and intermediate must
  not be similar in this case not common

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Transition State for Alkene Protonation

• Resembles carbocation intermediate
• Close in energy and adjacent on pathway
• Hammond Postulate says they should be similar in
  structure

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6.12 Mechanism of Electrophilic Addition
Rearrangements of Carbocations

• Carbocations undergo structural rearrangements
  following set patterns
• 1,2-H and 1,2-alkyl shifts occur
• Goes to give more stable carbocation
• Can go through less stable ions as intermediates

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