Organic Chemistry (6th Edition)
Organic Chemistry (6th Edition)
6th Edition
ISBN: 9781260119107
Author: Janice Gorzynski Smith
Publisher: McGraw Hill Education
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Chapter 1.8, Problem 21P

Convert each condensed formula to a Lewis structure.

a. CH 3 ( CH 2 ) 4 CH ( CH 3 ) 2

b. ( CH 3 ) 3 CCH ( OH ) CH 2 CH 3

c. ( CH 3 ) 2 CHCHO

d. ( HOCH 2 ) 2 CH ( CH 2 ) 3 C ( CH 3 ) 2 CH 2 CH 3

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Convert each condensed formula to a Lewis structure. a. CH3(CH2)4CH(CH3)2 b. (CH3)3CCH(OH)CH2CH3 c. (CH3)2CHCHO d. (HOCH2)2CH(CH2)3C(CH3)2CH2CH3
The Structure of Hydrocarbons 1. Draw the four carbon bonding patterns commonly seen in hydrocarbons and all other organic compounds. Construct the Lewis structures of the following compounds by combining the carbon atoms with the appropriate bonding patterns and the required number of hydrogen atoms. 2. a. hexane: CH,CH,CH,CH,CH,CH, b. 3-hexene: CH,CH,CH=CHCH,CH, c. 2-hexyne: CH,C=CCH,CH,CH, 3. There are three distinct bond angles formed in the four bonding patterns of carbon. What are they and in which bonding pattern(s) is each seen?
Draw the Lewis structure for each organic compound from its condensed structural formula.a. C2H4 b. CH3NH2 c. HCHOd. CH3CH2OH e. HCOOH

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Organic Chemistry (6th Edition)

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