EBK GET READY FOR ORGANIC CHEMISTRY
2nd Edition
ISBN: 8220100576379
Author: KARTY
Publisher: PEARSON
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Question
Chapter E, Problem E.11P
Interpretation Introduction
(a)
Interpretation:
The structure of
Concept introduction:
The structure of a molecule can be drawn from its IUPAC name. The IUPAC name consists of three parts. A root name specifies the number of carbons in the root chain or the size of the ring. The suffix, along with a specifier di, tri, etc. indicates the highest priority functional group, and the number and locations of its instances. Finally, any other
Interpretation Introduction
(b)
Interpretation:
The structure of
Concept introduction:
The structure of the compound can be drawn from its IUPAC name. The IUPAC name consists of three parts. A root name specifies the number of carbons in the root chain of the size of the ring. The suffix, along with a specifierdi, tri, etc. indicates the highest priority functional group, and the number and locations of its instances. Finally, the other functional groups are listed as prefixes with their locators.
Interpretation Introduction
(c)
Interpretation:
The structure of
Concept introduction:
The structure of a molecule can be drawn from its IUPAC name. The IUPAC name consists of three parts. A root name indicates the number of carbons in the root chain or the size of the ring. The suffix, along with a specifier di, tri, etc. indicates the highest priority functional group, and the number and locations of its instances. Finally, any other functional groups are listed as prefixes with their locators.
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Students have asked these similar questions
Draw the most stable chair conformation of 1-ethyl-1-methylcyclohexane, clearly showing the axial and equatorial substituents. [4]
Draw structures corresponding to the following IUPAC name for each of the following compounds; [5]
i) 4-Isopropyl-2,4,5-trimethylheptane
ii) trans-1-tert-butyl-4-ethylcyclohexane
iii) Cyclobutylcycloheptane
iv) cis-1,4-di-isopropylcyclohexane (chair conformation)
v) 3-Ethyl-5-isobutylnonane
Draw and name molecules that meet the following descriptions; [4]
a) An organic molecule containing 2 sp2 hybridised carbon and 1 sp-hybridised carbon atom.
b) A cycloalkene, C7H12, with a tetrasubstituted double bond.
Also answer question 2 from the image
H
14. Draw the line angle form of the following molecule make sure you use the proper
notation to indicate spatial positioning of atoms.
F
F
H
15. Convert the following condensed form to line angle form:
(CH3)3CCH2COCH2CON(CH2CH3)2
Chapter E Solutions
EBK GET READY FOR ORGANIC CHEMISTRY
Ch. E - Prob. E.1PCh. E - Prob. E.2PCh. E - Prob. E.3PCh. E - Prob. E.4PCh. E - Prob. E.5PCh. E - Prob. E.6PCh. E - Prob. E.7PCh. E - Prob. E.8PCh. E - Prob. E.9PCh. E - Prob. E.10P
Ch. E - Prob. E.11PCh. E - Prob. E.12PCh. E - Prob. E.13PCh. E - Prob. E.14PCh. E - Prob. E.15PCh. E - Prob. E.16PCh. E - Prob. E.17PCh. E - Prob. E.18PCh. E - Prob. E.19PCh. E - Prob. E.20PCh. E - Prob. E.21PCh. E - Prob. E.22PCh. E - Prob. E.23PCh. E - Prob. E.24PCh. E - Prob. E.25PCh. E - Prob. E.26PCh. E - Prob. E.27PCh. E - Prob. E.28PCh. E - Prob. E.29PCh. E - Prob. E.30PCh. E - Prob. E.31PCh. E - Prob. E.32PCh. E - Prob. E.33PCh. E - Prob. E.34PCh. E - Prob. E.35PCh. E - Prob. E.36PCh. E - Prob. E.37PCh. E - Prob. E.38PCh. E - Prob. E.39PCh. E - Prob. E.40PCh. E - Prob. E.41PCh. E - Prob. E.42PCh. E - Prob. E.43PCh. E - Prob. E.44PCh. E - Prob. E.45PCh. E - Prob. E.46PCh. E - Prob. E.47PCh. E - Prob. E.48P
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