practice for exam I

practice for exam I - Name_ 1. Draw the compounds described...

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Name ______________________________ 1. Draw the compounds described by the names given. cis -2-chloro-3-ethyl-1,1-dimethylcyclopropane 4-methylhexan-3-ol bicyclo[4.1.0]heptane 5-(1-methylethyl)-2,3,8-trimethylnonane 2. Give the names of the following compounds. Br 3. There are many constitutional isomers that can be made from the following empirical formula (C 5 H 10 O). Draw 5 of them. (15) 1
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4. For each pair, indicate the one that is the most acidic by writing its corresponding letter in the 2 nd column. In the column to the right concisely defend your choice by indicating the feature(s) that allowed you to make your choice. Acids to be compared most acidic? Brief reason for your choice H 3 C C H 2 O a b CH 3 F B F F H 3 C B CH 3 CH 3 g h H 2 O H 3 O + i j 5. Examine the neutral molecule below. For each of the indicated atoms, give the hybridization in the boxes provided. N O O C N O a b c d e a. b. c. d. e. 6.
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This note was uploaded on 10/03/2008 for the course CHEM 231 taught by Professor Kissling during the Fall '08 term at Binghamton University.

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practice for exam I - Name_ 1. Draw the compounds described...

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