Exam III - Chem 332 Exam III 4/15/2008

Info iconThis preview shows pages 1–4. Sign up to view the full content.

View Full Document Right Arrow Icon

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

View Full DocumentRight Arrow Icon

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

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

Unformatted text preview: Chem 332 Exam III 4/15/2008 NAME:_______________________________________ FIRST 2 LETTERS OF LAST NAME Part I fundamentals and mechanism 1. Give the IUPAC name for the following compounds.(8) O O H N H O CH 3 2. Give the functional group classification for the following compounds.(8) O O O N C H 3 C N CH 3 CH 3 H 3 C Cl O O 3. Draw each compound named in the boxes below.(8) Ethyl acetoacetate Any thioester 4. The following acyl compounds are shown to you in order from most electrophilic (top) to least electrophilic(bottom). Utilizing resonance structures and elemental properties, rationalize why this is the reactivity trend. (12) 1of 7 O S O O O O O 2of 7 5. For the following sets of compounds rank each according to the directions Indicate relative solubility in water using I for the highest solubility and III for the lowest solubility in water.(6) SET A NH 2 N NH Indicate relative boiling point, using I for the highest boiling point and III for the lowest boiling point.(6) SET B NH 2 N...
View Full Document

This note was uploaded on 06/19/2008 for the course CHEM 332 taught by Professor Kisslings during the Spring '08 term at Binghamton University.

Page1 / 11

Exam III - Chem 332 Exam III 4/15/2008

This preview shows document pages 1 - 4. Sign up to view the full document.

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