F06 midterm2

F06 midterm2 - ORGANIC CHEMISTRY 30B (Prof. Yves Rubin)...

Info iconThis preview shows pages 1–3. Sign up to view the full content.

View Full Document Right Arrow Icon
ORGANIC CHEMISTRY 30B (Prof. Yves Rubin) UCLA, FALL 2006 MIDTERM EXAM II On my honor, I have neither given nor received any aid on this exam ( Please, use ink for this first page! ): ____________________________ __________________________ Signature I. D. Number ____________________________ Full Name ( Please Print ! ) Question Points 1 (25) 2 (25) 3 (20) 4 (15) 5 (15) Total (100) =========
Background image of page 1

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

View Full DocumentRight Arrow Icon
EXAM II, Page 1 __________________ Name I. CONCEPTS / NOMENCLATURE 1. a) (4 points) Give an example of an excellent nucleophile and explain what factor gives it its nucleophilicity (no more than one short sentence please!): b) (6 points) Rank the following compounds by increasing basicity and give a short explanation for the difference: A B C MeO t -BuO H Trend: < < Why: c) (8 points) Name the following compounds by the IUPAC convention, unambiguously specifying any stereochemistry: OH OMe c) (7 points) Illustrate by an example the following terms seen in material covered this quarter: Ylide:
Background image of page 2
Image of page 3
This is the end of the preview. Sign up to access the rest of the document.

This test prep was uploaded on 04/05/2008 for the course CHEM 30B taught by Professor Rubin during the Fall '05 term at UCLA.

Page1 / 6

F06 midterm2 - ORGANIC CHEMISTRY 30B (Prof. Yves Rubin)...

This preview shows document pages 1 - 3. Sign up to view the full document.

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