CHEM 110 Lecture Notes - Lecture 21: Trigonal Planar Molecular Geometry, Saturated And Unsaturated Compounds, Pi Bond

24 views2 pages
lionel.angibeaud and 39534 others unlocked
CHEM 110 Full Course Notes
37
CHEM 110 Full Course Notes
Verified Note
37 documents

Document Summary

Electrophilic additions to alkenes: substrate: molecule that undergoes addition (alkene, electrophile: hydrogen of h-x (or other s+ of x-x reagent, nucleophile: attacking lewis base (pi bond, leaving group: displaced halide or other x of strong acid. *addition reactions = nucleophile attacks electrophile (with displacement of lg, which then. Attack" adjacent carbon) (1) c=c attack on h-x, formation of c-h pi bond & c+ (2) x- attack on c+, formation of c-x pi bond. Addition mechanism: (1) c=c attack on h-x, formation of c-h sigma bond & c+ (2) x- attack on c+, formation of c-x sigma bond (3) c-oh2+ loses h+ to water/solvent: addition of diatomics: addition of x-x. X2 addition mechanism: c=c attack on x-x, formation of c-x sigma bond & cyclic cation, x- attack on cyclic cation, formation of c-x sigma bond. Hydrogenation: hydrogenation: the addition of hydrogen to an unsaturated compound, hydrogen attached to metal surface forced on same side bc added at same time.

Get access

Grade+
$40 USD/m
Billed monthly
Grade+
Homework Help
Study Guides
Textbook Solutions
Class Notes
Textbook Notes
Booster Class
10 Verified Answers
Class+
$30 USD/m
Billed monthly
Class+
Homework Help
Study Guides
Textbook Solutions
Class Notes
Textbook Notes
Booster Class
7 Verified Answers

Related textbook solutions

Related Documents

Related Questions