ORGANIC CHEMISTRY SAPLING ACCESS + ETEX
6th Edition
ISBN: 9781319306977
Author: LOUDON
Publisher: INTER MAC
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Question
Chapter 7, Problem 7.75AP
Interpretation Introduction
(a)
Interpretation:
The total number of stereochemical ways by which the two rings in a bridged bicyclic compound can be joined is to be stated.
Concept introduction:
A molecule which contains two rings joined together is known as bicyclic molecule. The compound in which the two rings share three or more than three atoms and the two bridgehead atoms are separated through a bridge possessing at least one atom is known as bridged bicyclic compound.
Interpretation Introduction
(b)
Interpretation:
Among the bridged bicyclic compounds,
Concept introduction:
A molecule which contains two rings joined together is known as bicyclic molecule. The compound in which the two rings share three or more than three atoms and the two bridgehead atoms are separated through a bridge possessing at least one atom is known as bridged bicyclic compound.
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Concentration
Trial1
Concentration of iodide solution (mA)
255.8
Concentration of thiosulfate solution (mM)
47.0
Concentration of hydrogen peroxide solution (mM)
110.1
Temperature of iodide solution ('C)
25.0
Volume of iodide solution (1) used (mL)
10.0
Volume of thiosulfate solution (5:03) used (mL)
Volume of DI water used (mL)
Volume of hydrogen peroxide solution (H₂O₂) used (mL)
1.0
2.5
7.5
Time (s)
16.9
Dark blue
Observations
Initial concentration of iodide in reaction (mA)
Initial concentration of thiosulfate in reaction (mA)
Initial concentration of hydrogen peroxide in reaction (mA)
Initial Rate (mA's)
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
Chapter 7 Solutions
ORGANIC CHEMISTRY SAPLING ACCESS + ETEX
Ch. 7 - Prob. 7.1PCh. 7 - Prob. 7.2PCh. 7 - Prob. 7.3PCh. 7 - Prob. 7.4PCh. 7 - Prob. 7.5PCh. 7 - Prob. 7.6PCh. 7 - Prob. 7.7PCh. 7 - Prob. 7.8PCh. 7 - Prob. 7.9PCh. 7 - Prob. 7.10P
Ch. 7 - Prob. 7.11PCh. 7 - Prob. 7.12PCh. 7 - Prob. 7.13PCh. 7 - Prob. 7.14PCh. 7 - Prob. 7.15PCh. 7 - Prob. 7.16PCh. 7 - Prob. 7.17PCh. 7 - Prob. 7.18PCh. 7 - Prob. 7.19PCh. 7 - Prob. 7.20PCh. 7 - Prob. 7.21PCh. 7 - Prob. 7.22PCh. 7 - Prob. 7.23PCh. 7 - Prob. 7.24PCh. 7 - Prob. 7.25PCh. 7 - Prob. 7.26PCh. 7 - Prob. 7.27PCh. 7 - Prob. 7.28PCh. 7 - Prob. 7.29PCh. 7 - Prob. 7.30PCh. 7 - Prob. 7.31PCh. 7 - Prob. 7.32PCh. 7 - Prob. 7.33PCh. 7 - Prob. 7.34APCh. 7 - Prob. 7.35APCh. 7 - Prob. 7.36APCh. 7 - Prob. 7.37APCh. 7 - Prob. 7.38APCh. 7 - Prob. 7.39APCh. 7 - Prob. 7.40APCh. 7 - Prob. 7.41APCh. 7 - Prob. 7.42APCh. 7 - Prob. 7.43APCh. 7 - Prob. 7.44APCh. 7 - Prob. 7.45APCh. 7 - Prob. 7.46APCh. 7 - Prob. 7.47APCh. 7 - Prob. 7.48APCh. 7 - Prob. 7.49APCh. 7 - Prob. 7.50APCh. 7 - Prob. 7.51APCh. 7 - Prob. 7.52APCh. 7 - Prob. 7.53APCh. 7 - Prob. 7.54APCh. 7 - Prob. 7.55APCh. 7 - Prob. 7.56APCh. 7 - Prob. 7.57APCh. 7 - Prob. 7.58APCh. 7 - Prob. 7.59APCh. 7 - Prob. 7.60APCh. 7 - Prob. 7.61APCh. 7 - Prob. 7.62APCh. 7 - Prob. 7.63APCh. 7 - Prob. 7.64APCh. 7 - Prob. 7.65APCh. 7 - Prob. 7.66APCh. 7 - Prob. 7.67APCh. 7 - Prob. 7.68APCh. 7 - Prob. 7.69APCh. 7 - Prob. 7.70APCh. 7 - Prob. 7.71APCh. 7 - Prob. 7.72APCh. 7 - Prob. 7.73APCh. 7 - Prob. 7.74APCh. 7 - Prob. 7.75AP
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