$35
for 3.5-Hours
Acid/Base Reactions
and Resonance
Review Session Details
- Learn to draw resonance forms (and be able to identify major and minor structures)
- Learn to assess/draw electron pushing arrows for acid/base reactions
- Assessing a lone pair's strength
- Understand how lone pairs are affected by resonance, electronegativity, atom size, inductive effect and s-character
- Assessing acidity of various hydrogen atoms
- Understand how to use pKa to assess acidity
- Determine the favoured equilibrium direction for acid/base reactions
- Drawing mechanism arrows for acid/base reactions
- Draw most dominant charge using pKa and pH
- All students attending Review Session will receive "Midterm 2 Package" containing past uOttawa Professor midterms!
CHM1321/1721: Resonance, Lone Pair Strength and Acid-Base Chemistry
$40.00
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$35
for 3.5-Hours
π-bonds as
Nucleophiles
Review Session Details
- Assessment of carbocation stability
- Learning when/how to conduct 1,2 rearrangement reaction with carbocations
- Alkene/alkyne addition reactions in the presence of strong acid (i.e. ALL Markovnikov reactions)
- Hydroboration reaction (with thorough explanation of mechanism, stereochemistry and regioselectivity)
- Formation of epoxides using alkene (with thorough explanation of mechanism, stereochemistry and regioselectivity)
- Halogenation reaction using alkene/alkynes (with thorough explanation of mechanism, stereochemistry and regioselectivity)
- Understanding how to use Grignard reagents as nucleophiles
- Understanding how to use Boron/Aluminum hydrate reagents as nucleophiles
- Reduction of carbonyls using Boron/Aluminum hydrate reagents
- Alkylation of carbonyls using Grignard reagents
- ALL complex mechanism will be simplified into groups and necessary theory will be discussed.
- All students attending Review Session will receive "Midterm 2 Package" containing past uOttawa Professor midterms!
CHM1321/1721: π-bonds Electrophile Reactions
$40.00
Related products
$35
for 3.5-Hours
π-bonds as
Electrophiles
Review Session Details
- Assessment of carbocation stability
- Learning when/how to conduct 1,2 rearrangement reaction with carbocations
- Alkene/alkyne addition reactions in the presence of strong acid (i.e. ALL Markovnikov reactions)
- Hydroboration reaction (with thorough explanation of mechanism, stereochemistry and regioselectivity)
- Formation of epoxides using alkene (with thorough explanation of mechanism, stereochemistry and regioselectivity)
- Halogenation reaction using alkene/alkynes (with thorough explanation of mechanism, stereochemistry and regioselectivity)
- ALL complex mechanism will be simplified into groups and necessary theory will be discussed.
- All students attending Review Session will receive "Midterm and Final Exam Package" containing past uOttawa Professor midterms and some finals!
CHM1321/1721: π-bonds as Nucleophiles
$40.00
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