Student Study Guide and Solutions Manual T/A Organic Chemistry
2nd Edition
ISBN: 9781118647950
Author: David R. Klein
Publisher: WILEY
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Question
Chapter 13, Problem 53IP
Interpretation Introduction
Interpretation:
The structure of the compound should be identified from given molecular formula.
Concept introduction:
Nuclear Magnetic Resonance (NMR) spectroscopy is a technique used for determining molecular structure of the organic molecule as well the content and purity of the molecule.
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Students have asked these similar questions
Draw the condensed or line-angle structure for an alkene with the formula C5H10.
Note: Avoid selecting cis-/trans- isomers in this exercise.
Draw two additional condensed or line-angle structures for alkenes with the formula C5H10.
Record the name of the isomers in Data Table 1.
Repeat steps for 2 cyclic isomers of C5H10
Explain why the following names of the structures are incorrect.
CH2CH3
CH3-C=CH-CH2-CH3
a. 2-ethyl-2-pentene
CH3
|
CH3-CH-CH2-CH=CH2
b. 2-methyl-4-pentene
Draw the line-angle formula of cis-2,3-dichloro-2-pentene. Then, draw the line-angle formula of trans-2,3-dichloro-2-pentene below.
Draw the dash-wedge formula of cis-1,3-dimethylcyclohexane. Then, draw the dash-wedge formula of trans-1,3-dimethylcyclohexane below.
Chapter 13 Solutions
Student Study Guide and Solutions Manual T/A Organic Chemistry
Ch. 13.1 - Prob. 1LTSCh. 13.1 - Prob. 1PTSCh. 13.1 - Prob. 2ATSCh. 13.1 - Prob. 3CCCh. 13.2 - Prob. 4CCCh. 13.2 - Prob. 2LTSCh. 13.2 - Prob. 5PTSCh. 13.2 - Prob. 6ATSCh. 13.3 - Prob. 7CCCh. 13.3 - Prob. 8CC
Ch. 13.4 - Prob. 3LTSCh. 13.4 - Prob. 9PTSCh. 13.4 - Prob. 10ATSCh. 13.4 - Prob. 11ATSCh. 13.4 - Prob. 4LTSCh. 13.4 - Prob. 12PTSCh. 13.4 - Prob. 13ATSCh. 13.6 - Prob. 5LTSCh. 13.6 - Prob. 14PTSCh. 13.6 - Prob. 15ATSCh. 13.6 - Prob. 16ATSCh. 13.6 - Prob. 17ATSCh. 13.7 - Prob. 18CCCh. 13.9 - Prob. 6LTSCh. 13.9 - Prob. 19PTSCh. 13.9 - Prob. 20ATSCh. 13.9 - Prob. 21CCCh. 13.10 - Prob. 7LTSCh. 13.10 - Prob. 22PTSCh. 13.10 - Prob. 23ATSCh. 13.13 - Prob. 8LTSCh. 13.13 - Prob. 24PTSCh. 13.13 - Prob. 25ATSCh. 13.13 - Prob. 26ATSCh. 13.13 - Prob. 27CCCh. 13.13 - Prob. 9LTSCh. 13.13 - Prob. 28PTSCh. 13.13 - Prob. 29ATSCh. 13 - Prob. 30PPCh. 13 - Prob. 31PPCh. 13 - Prob. 32PPCh. 13 - Prob. 33PPCh. 13 - Prob. 34PPCh. 13 - Prob. 35PPCh. 13 - Prob. 36PPCh. 13 - Prob. 37PPCh. 13 - Prob. 38PPCh. 13 - Prob. 39PPCh. 13 - Prob. 40PPCh. 13 - Prob. 41PPCh. 13 - Prob. 42PPCh. 13 - Prob. 43PPCh. 13 - Prob. 44PPCh. 13 - Prob. 45PPCh. 13 - Prob. 46PPCh. 13 - Prob. 47PPCh. 13 - Prob. 48PPCh. 13 - Prob. 49PPCh. 13 - Prob. 50PPCh. 13 - Prob. 51IPCh. 13 - Prob. 52IPCh. 13 - Prob. 53IPCh. 13 - Prob. 54IPCh. 13 - Prob. 55IPCh. 13 - Prob. 56IPCh. 13 - Prob. 57IPCh. 13 - Prob. 58IPCh. 13 - Prob. 59IPCh. 13 - Prob. 60IPCh. 13 - Prob. 61IPCh. 13 - Prob. 62IPCh. 13 - Prob. 63IP
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- Record the amounts measured and calculate the percent yield for Part 2 in the table below. Dicyclopentadiene measured in volume Cyclopentadiene measured in grams 0 Measured Calculated Mol Yield Mass (g) or Volume (mL) Mass (g) or Volume (ml) 0.6 2.955 Part 2 Measurements and Results Record the amounts measured and calculate the percent yield for Part 2 in the table below. 0.588 0.0044 2.868 0.0434 N/A Table view List view Measured Calculated Mol $ Yield Melting Point (C) Mass (g) or Volume (ml) Mass (g) or Volume (ml.) Cyclopentadiene 0.1 0.08 0.001189 measured in volume Maleic Anhydride 0.196 N/A cis-norbornene-5,6-endo- dicarboxylic anhydride 0.041 0.0002467 N/A N/A N/A 0.002 N/A N/A 128arrow_forwardDraw the condensed structural formula and line-angle formula for each: 2,3-dimethylheptane 3-bromo-2-pentanol 3-isopropyl-2-hexene 4-chlorobutanoic acidarrow_forwardRecord the IUPAC names for each of the structures shown below. a) b) c) OH d) OH e)arrow_forward
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