CHEM 211 Lecture 32: Addition II

20 views2 pages

Document Summary

Two ways we learned alcohols can be formed: acid-catalyzed hydration. No rearrangement occurs: this is because there is never really a carbocation formed. Alcohols from alkenes through hydroboration-oxidation: non-markovnikov syn. Hydration: now we can put the alcohol on the carbon with the more h"s. Other types of adding alcohol adds the oh onto the carbon with the more substituents: and the h goes onto the carbon with the more substituents (non-markovnikovian) Hydroboration: synthesis of alkylboranes: alkylborane = boron attached to a carbon. Mechanism for hydroboration: four atom concerted transition state. Bond between h and br partially broken. Bond between h and c partially formed. Bond between br and c partially formed: syn addition. To make a non-maokovnikov br: add h2o2 and heat. Addition of br and cl to alkenes: addition of x-x (ex. Cl2, br2) across of c=c bond: forms a racematic solution, always anti-addition. Trans-2-butene + b2: trans trans, gives you meso compound.

Get access

Grade+20% off
$8 USD/m$10 USD/m
Billed $96 USD annually
Grade+
Homework Help
Study Guides
Textbook Solutions
Class Notes
Textbook Notes
Booster Class
40 Verified Answers
Class+
$8 USD/m
Billed $96 USD annually
Class+
Homework Help
Study Guides
Textbook Solutions
Class Notes
Textbook Notes
Booster Class
30 Verified Answers

Related textbook solutions

Related Documents

Related Questions