General, Organic, and Biological Chemistry - 4th edition
4th Edition
ISBN: 9781259883989
Author: by Janice Smith
Publisher: McGraw-Hill Education
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Textbook Question
Chapter 13.1, Problem 13.1PP
Convert each condensed structure to a complete structure with all atoms, bond lines, and lone pairs drawn in.
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I have given you a condensed structure. You need to convert it to an accurate bond-line
structure.
CH3
CH3-CH-CH2-CH-CH₂-C-H
12-CH-CH2₂-C-1
CI
Draw (as bond-line structures) isomers of this compound where you only move the chlorine
atom.
Draw four isomers of the original compound that would have a five carbon chain as the longest
chain. [Note: there would be many isomers that will satisfy this. Find any four.]
Using the original molecule (and looking at the carbon next to the aldehyde carbonyl) what
would be the charge on that carbon if I removed an H atom and left behind the pair of electrons?
Circle the best answer
Positive
Negative
Neutral
In the space below, draw that structure (from the sentence above) as a bond-line structure. Then,
draw a resonance structure for this ion and be sure to add curved arrows to show the movement
of electrons.
=
ORGANIC CHEMISTRY
Drawing a skeletal structure from a condensed structure
Draw a skeletal ("line") structure of this molecule:
CH3
i
CH3 C-CH₂-
-C-CH3
CH3
—
Rewrite each of these structures as a condensed structure.
H F\H H
H-C-Ċ-Ċ –Ċ-H
H FHH
condensed structure: CH3CF2CH2CH3
H H
нНН
H.
H-С—С—С—Н
H O
H.
1
H.
condensed structure: CH-3-CH-CH3
Chapter 13 Solutions
General, Organic, and Biological Chemistry - 4th edition
Ch. 13.1 - Convert each condensed structure to a complete...Ch. 13.1 - Prob. 13.1PCh. 13.1 - Complete the structure of zingiberene, a component...Ch. 13.2 - Prob. 13.2PPCh. 13.2 - Prob. 13.3PCh. 13.2 - Prob. 13.3PPCh. 13.2 - Prob. 13.4PPCh. 13.3 - Prob. 13.5PPCh. 13.3 - Prob. 13.4PCh. 13.3 - Prob. 13.6PP
Ch. 13.3 - Prob. 13.5PCh. 13.3 - Prob. 13.6PCh. 13.3 - Prob. 13.7PCh. 13.3 - Prob. 13.8PCh. 13.6 - Prob. 13.7PPCh. 13.6 - Prob. 13.9PCh. 13.6 - What products is formed in each of the following...Ch. 13.6 - Prob. 13.9PPCh. 13.6 - What product is formed when l-pentene (CH3CH2CH2CH...Ch. 13.7 - Prob. 13.11PCh. 13.8 - Prob. 13.10PPCh. 13.8 - Prob. 13.12PCh. 13.8 - Prob. 13.13PCh. 13.10 - Prob. 13.11PPCh. 13.10 - Prob. 13.14PCh. 13.11 - Prob. 13.15PCh. 13.12 - Prob. 13.16PCh. 13.13 - Prob. 13.17PCh. 13.13 - Prob. 13.18PCh. 13 - Anethole, the major constituent of anise oil, is...Ch. 13 - Prob. 20PCh. 13 - What is the molecular formula for a hydrocarbon...Ch. 13 - Prob. 22PCh. 13 - Prob. 23PCh. 13 - Prob. 24PCh. 13 - Prob. 25PCh. 13 - Prob. 26PCh. 13 - Give the IUPAC name for each molecule depicted in...Ch. 13 - Give the IUPAC name for each molecule depicted in...Ch. 13 - Give the IUPAC name for each compound. a....Ch. 13 - Give the IUPAC name for each compound. d....Ch. 13 - Give the IUPAC name for each alkene.Ch. 13 - Give the I UP AC name for each alkene.Ch. 13 - Give the IUPAC name for each cyclic compound.Ch. 13 - Give the IUPAC name for each cyclic compound.Ch. 13 - Give the structure corresponding to each IUPAC...Ch. 13 - Prob. 36PCh. 13 - Each of the following IUPAC names is incorrect....Ch. 13 - Each of the following IUPAC names is incorrect....Ch. 13 - Prob. 39PCh. 13 - Prob. 40PCh. 13 - Prob. 41PCh. 13 - Prob. 42PCh. 13 - Prob. 43PCh. 13 - Label the carbon-carbon double bond as cis or...Ch. 13 - Prob. 45PCh. 13 - Prob. 46PCh. 13 - Prob. 47PCh. 13 - Prob. 48PCh. 13 - Prob. 49PCh. 13 - Prob. 50PCh. 13 - Prob. 51PCh. 13 - Prob. 52PCh. 13 - Prob. 53PCh. 13 - Prob. 54PCh. 13 - What alkyd halide is formed when each alkene is...Ch. 13 - Prob. 56PCh. 13 - Prob. 57PCh. 13 - Prob. 58PCh. 13 - What alkene is needed as a starting material to...Ch. 13 - Prob. 60PCh. 13 - Prob. 61PCh. 13 - Prob. 62PCh. 13 - Prob. 63PCh. 13 - Prob. 64PCh. 13 - Prob. 65PCh. 13 - Prob. 66PCh. 13 - Prob. 67PCh. 13 - Prob. 68PCh. 13 - Prob. 69PCh. 13 - Prob. 70PCh. 13 - Prob. 71PCh. 13 - Prob. 72PCh. 13 - Prob. 73PCh. 13 - Are o-bromochlorobenzene and m-bromochlorobenzene...Ch. 13 - Give the structure corresponding to each IUPAC...Ch. 13 - Give the structure corresponding to each IUPAC...Ch. 13 - Prob. 77PCh. 13 - Prob. 78PCh. 13 - Prob. 79PCh. 13 - Prob. 80PCh. 13 - Prob. 81PCh. 13 - Prob. 82PCh. 13 - Prob. 83PCh. 13 - Prob. 84PCh. 13 - Prob. 85PCh. 13 - Eleostearic acid is an unsaturated fatty acid...Ch. 13 - Prob. 87PCh. 13 - Prob. 88PCh. 13 - Prob. 89PCh. 13 - Prob. 90PCh. 13 - Prob. 91PCh. 13 - Prob. 92PCh. 13 - Prob. 93PCh. 13 - Prob. 94PCh. 13 - Answer the following questions about compound A,...Ch. 13 - Prob. 96PCh. 13 - Answer the following questions about alkene C,...Ch. 13 - Prob. 98PCh. 13 - Prob. 99PCh. 13 - Prob. 100PCh. 13 - Prob. 101CPCh. 13 - Prob. 102CP
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- = ORGANIC CHEMISTRY Drawing a skeletal structure from a condensed structure Draw a skeletal ("line") structure of this molecule: OH CH3 -C-CH₂-CH=CH₂ OHarrow_forwardProvide a line structure for the following condensed structure: (CH3)2CH(CH2)2CCH(CH3)2CH(CH3)(CH,CH3)(CH2)3CH3arrow_forwardDraw the structural condensed formula of CHCCH(OH)CH3. Include all lone pairs and charges as appropriate. Drawingarrow_forward
- Which of the following is the correct condensed structure for the following compound? O CH3C(CH3)2(CH2)2(CH)BrC(CH3)2 O CH3CH3CH3C(CH₂)2C(CH3)2CHBr O (CH3)3C(CH₂)3BrCHCH³CH3 O CH3CH₂CH3C(CH₂)₂CHBrCHCH3CH³ O (CH3)3C(CH₂)₂CHBrCH(CH3)2arrow_forward5) Complete the expanded structural formulas for these molecules with double bonds by bonding the correct number of H atoms to each C. You need to make sure that each C has 4 bonds. сн c=c-E-c 4 H C₂ C=C C-C сarrow_forwardADVANCED MATERIAL Drawing a skeletal structure from a condensed structure CH-CH3 CH3 C-CH-CH,-C- -CH3 C Click and drag to start drawing a structure. to C2 IIarrow_forward
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