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Hydroboration oxidation - PowerPoint PPT Presentation

p. 251

p. 251

p. 251. Alkenes & Alkynes. Prepapration of alkenes 1. Dehydrohalogenation 2. Dehydration. Alkenes & Alkynes. Reactions of alkenes & alkynes A. Electrophilic Additions to Alkenes Hydrohalogenation 2. Halogenation Halohydrins 4. Hydration. Alkenes & Alkynes.

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666 views • 66 slides
p. 251

p. 251

p. 251. Alkenes & Alkynes. Prepapration of alkenes 1. Dehydrohalogenation 2. Dehydration. Alkenes & Alkynes. Reactions of alkenes & alkynes A. Electrophilic Additions Hydrohalogenation i. alkenes ii. alkynes 2. Halogenation i. alkenes ii. alkynes Halohydrins i. alkenes

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1k views • 63 slides
p. 251

p. 251

p. 251. Alkenes & Alkynes. Prepapration of alkenes 1. Dehydrohalogenation 2. Dehydration. Alkenes & Alkynes. Reactions of alkenes & alkynes A. Electrophilic Additions Hydrohalogenation i. alkenes ii. alkynes 2. Halogenation i. alkenes ii. alkynes Halohydrins i. alkenes

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648 views • 63 slides
ALKENES/ALKYNES, REACTIONS

ALKENES/ALKYNES, REACTIONS

ALKENES/ALKYNES, REACTIONS. Elimination, basics. Elimination, basics. Addition of X 2. Addition of X 2. Addition of HX. Addition of HX. Addition of X 2 in H 2 O. Addition of X 2 in H 2 O. Addition of X 2 in H 2 O. Addition of X 2 in H 2 O. Oxymercuration , (H 2 O addition).

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873 views • 55 slides
Chapter 5. Alkenes and Alkynes II: Reactions

Chapter 5. Alkenes and Alkynes II: Reactions

Chapter 5. Alkenes and Alkynes II: Reactions. Elimination Reactions. Addition Reactions. Addition of Halogens. Examples. Mechanism. Halohydrin Formation. Mechanism. Orientation of the OH toward the more stable cabocation ( f ollows Markovnikov addition). Hydrogenation.

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570 views • 34 slides
Chapter 5

Chapter 5

Chapter 5. Addition Reaction of Alkenes. Addition of Halogens to Alkenes. Addition of Cl 2 and Br 2 to give vicinal dihalides. The other halogens are not commonly used because F 2 is too reactive and I 2 is not reactive enough

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478 views • 33 slides
Chapter 5

Chapter 5

Chapter 5. Addition Reaction of Alkenes. Addition of Halogens to Alkenes. Addition of Cl 2 and Br 2 to give vicinal dihalides. The other halogens are not commonly used because F 2 is too reactive and I 2 is not reactive enough

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394 views • 33 slides
Both bonding electrons remain with one product fragment in this kind of reaction.

Both bonding electrons remain with one product fragment in this kind of reaction.

0. Both bonding electrons remain with one product fragment in this kind of reaction. Homolytic bond cleavage Heterolytic bond cleavage Radical reaction More than one of the above is true None of the above. 0. Which of the following is not a Lewis base?. A B C D. 0.

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580 views • 23 slides
Chapter 9 & 10

Chapter 9 & 10

Chapter 9 & 10. Hydrogenation. Section 10.2. Hydrogenation. Hydrogenation. Hydroboration. Anti-Markovnikov Addition. Borane. Hydroboration Mechanism. Reaction Coordinate Diagram. Energy. Reaction Coordinate. Hydroboration. Hydroboration. Oxidation.

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621 views • 15 slides

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