CHM138H1 Chapter all: Acids And Bases

152 views8 pages
1 Dec 2016
School
Department
Course
Professor
skyelephant476 and 39509 others unlocked
CHM136H1 Full Course Notes
34
CHM136H1 Full Course Notes
Verified Note
34 documents

Document Summary

Section 3. 1: intro to br nsted-lowry acids and bases: a br nsted-lowry acid is a proton donor, while a br nsted-lowry base is a proton acceptor. Bronzed-lowry deals in proton transfers: br nsted-lowry acid-base reactions create a conjugate acid and a con- jugate base. Section 3. 4: br nsted-lowry acidity: qualitative perspective: relative acidity is predicable by analyzing the structure of the conjugate base with out using pka values. If a- is very stable, then ha must be a strong acid. For elements in the same row of the periodic table, electronegativity is the dominant effect. For elements in the same column, size is the dominant effect. Thus, it is makes a acidic compound relative to deprotonated carbon: resonance a negative charge is stabilized by resonance. Thus a molecule with a carboxyl group is more acidic because the charge has resonance over the ho-c=o group: induction electron-withdrawing groups, such as halogens, stabilize a nearby negative charge via induction.

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

Related Documents

Related Questions