EBK ORGANIC CHEMISTRY
6th Edition
ISBN: 8220103151757
Author: LOUDON
Publisher: MAC HIGHER
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Chapter 10, Problem 10.7P
Interpretation Introduction
Interpretation:
The major
Concept introduction:
The dehydration of alcohol leads to the formation of the alkene. This dehydration can be done acid-catalyzed mechanism. In this mechanism first step is the abstraction of a proton by the hydroxide group. The second step is the removal of water to give an intermediate “carbocation”. The third step is the generation of an alkene by the removal of
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As shown in Scheme 4 and in the image below, the exo-cycloadduct is presented in 3-D. Select the correct 2-D depiction of the
same molecule.
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C
a
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b B
C
A
e
C
d D
A
E
exo-product
B
D
E
Draw the alkene structure that produced the following compounds in a ozonolysis reaction as specified.
1. O3
2. (CH3)2S
You do not have to consider stereochemistry.
You do not have to explicitly draw H atoms.
In cases where there is more than one answer, just draw one.
Draw the geometric isomers (if any) of the following alkenes. Identify the geometric isomer as either cisor transor as either Eor Z, where applicable.
a.BrHC=CHBr
c. (HO)(CH3CH2)C=CH(CH2CH3)
b.ClHC=CCl2
d. (I)(CH3CH2CH2)C=C(CH2CH3)(CH3)
Chapter 10 Solutions
EBK ORGANIC CHEMISTRY
Ch. 10 - Prob. 10.1PCh. 10 - Prob. 10.2PCh. 10 - Prob. 10.3PCh. 10 - Prob. 10.4PCh. 10 - Prob. 10.5PCh. 10 - Prob. 10.6PCh. 10 - Prob. 10.7PCh. 10 - Prob. 10.8PCh. 10 - Prob. 10.9PCh. 10 - Prob. 10.10P
Ch. 10 - Prob. 10.11PCh. 10 - Prob. 10.12PCh. 10 - Prob. 10.13PCh. 10 - Prob. 10.14PCh. 10 - Prob. 10.15PCh. 10 - Prob. 10.16PCh. 10 - Prob. 10.17PCh. 10 - Prob. 10.18PCh. 10 - Prob. 10.19PCh. 10 - Prob. 10.20PCh. 10 - Prob. 10.21PCh. 10 - Prob. 10.22PCh. 10 - Prob. 10.23PCh. 10 - Prob. 10.24PCh. 10 - Prob. 10.25PCh. 10 - Prob. 10.26PCh. 10 - Prob. 10.27PCh. 10 - Prob. 10.28PCh. 10 - Prob. 10.29PCh. 10 - Prob. 10.30PCh. 10 - Prob. 10.31PCh. 10 - Prob. 10.32PCh. 10 - Prob. 10.33PCh. 10 - Prob. 10.34PCh. 10 - Prob. 10.35PCh. 10 - Prob. 10.36PCh. 10 - Prob. 10.37PCh. 10 - Prob. 10.38PCh. 10 - Prob. 10.39APCh. 10 - Prob. 10.40APCh. 10 - Prob. 10.41APCh. 10 - Prob. 10.42APCh. 10 - Prob. 10.43APCh. 10 - Prob. 10.44APCh. 10 - Prob. 10.45APCh. 10 - Prob. 10.46APCh. 10 - Prob. 10.47APCh. 10 - Prob. 10.48APCh. 10 - Prob. 10.49APCh. 10 - Prob. 10.50APCh. 10 - Prob. 10.51APCh. 10 - Prob. 10.52APCh. 10 - Prob. 10.53APCh. 10 - Prob. 10.54APCh. 10 - Prob. 10.55APCh. 10 - Prob. 10.56APCh. 10 - Prob. 10.57APCh. 10 - Prob. 10.58APCh. 10 - Prob. 10.59APCh. 10 - Prob. 10.60APCh. 10 - Prob. 10.61APCh. 10 - Prob. 10.62APCh. 10 - Prob. 10.63APCh. 10 - Prob. 10.64APCh. 10 - Prob. 10.65APCh. 10 - Prob. 10.66APCh. 10 - Prob. 10.67APCh. 10 - Prob. 10.68APCh. 10 - Prob. 10.69APCh. 10 - Prob. 10.70AP
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- Provide an IUPAC name for the compound below. ball & stick 0O labels (Specify (E) or (Z) stereochemistry, if relevant, for straight chain alkenes only. It is not necessary to use italics in writing compound names. Pay attention to commas, dashes, and parentheses. )arrow_forwardDraw the structure for an alkene that gives the following reaction product. 7 CH2l2, Zn/Cu Ignore alkene stereochemistry. • You do not have to explicitly draw H atoms. • In cases where there is more than one answer, just draw one. / [F ?arrow_forwardH₂N- -Br H₂C Provide the locant and substituent in the order that they will be written in the name. The parent name is (old IUPAC version) or (new IUPAC version).arrow_forward
- It is sometimes necessary to isomerize a cis alkene to a trans alkene in asynthesis, a process that cannot be accomplished in a single step. Usingthe reactions , devise a stepwise method to convert cis-but-2-ene to trans-but-2-ene.arrow_forwardProvide an IUPAC name for each of the compounds shown. (Specify (E)/(Z) stereochemistry, if relevant, for straight chain alkenes only. Pay attention to commas, dashes, etc.) Br. H C=C CH3 H₂C-CH₂ CI CH₂CH3arrow_forwardDraw the alkene that would react with the reagent given to account for the product formed. ? + + H₂O **** H₂S04 • You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. • In cases where there is more than one answer, just draw one. CH3 CH3 CHCCH3 | | OH CH3 +1arrow_forward
- Write a structural formula and give two acceptable IUPAC names for each alkene of molecular formula C7H14 that has a tetrasubstituted double bond.arrow_forwardDraw the alkene that would react with the reagent given to account for the product formed. CH3 HCI CH3 CHCCH, ? + Či CH3 You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. • In cases where there is more than one answer, just draw one.arrow_forwardDraw the structural formula for all the alkenes with the indicated molecular formula that, without undergoing a rearrangement, produce the compound shown as a major product. Br. C7H12 Br2/H₂O OH . You do not have to consider stereochemistry. • If more than one structure fits the description, draw them all. ⚫ Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. Separate structures with + signs from the drop-down menu. 0 ? F ChemDoodle Previous Nextarrow_forward
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