12-10 - 12/10/2010 Final Exam Thurs, Dec 16 8:00-10:45 AM...

Info iconThis preview shows pages 1–2. Sign up to view the full content.

View Full Document Right Arrow Icon
12/10/2010 1 Final Exam Thurs, Dec 16 8:00-10:45 AM Models and one 5” x 8” index card permitted No calculators or other electronic devices Rooms will be announced on Blackboard and Course 1 Rooms will be announced on Blackboard and Course Website by Monday. Review Session Day Time Wed Dec 15 –CLC 8 pm Tools for understanding, remembering, and predicting reactions. Synthesis Stereochemistry Additi /Eli i ti /S b tit ti 3 Addition/Elimination/Substitution Electrophiles/Nucleophiles Lewis Acids/Bases Resonance Induction/Hyperconjugation Electronegativity Structure Addition of NaHCO 3 to both A and B yields CO 2 . One diastereomer forms a compound with a new carbon structure C . One diastereomer does not. B NaHCO 3 /H 2 O CO 2 NaHCO 3 /H 2 O CO 2 + ? + ? 4 A Why is CO 2 formed? a. Deprotonation of the carboxylic acid by HCO 3 - b. Decarboxylation of the norbornene carboxylic acid + HCO 3 - H 2 O + CO 2 + H 2 CO 3 One diastereomer forms a compound with a new carbon structure C . One diastereomer does not. Which atom is the most nucleophilic (Lewis base)?
Background image of page 1

Info iconThis preview has intentionally blurred sections. Sign up to view the full version.

View Full DocumentRight Arrow Icon
Image of page 2
This is the end of the preview. Sign up to access the rest of the document.

This note was uploaded on 01/07/2011 for the course CHE 321 taught by Professor Fowler/sampson during the Spring '08 term at SUNY Stony Brook.

Page1 / 4

12-10 - 12/10/2010 Final Exam Thurs, Dec 16 8:00-10:45 AM...

This preview shows document pages 1 - 2. Sign up to view the full document.

View Full Document Right Arrow Icon
Ask a homework question - tutors are online