PRINCIPLES OF MODERN CHEMISTRY-OWLV2
8th Edition
ISBN: 9781305271609
Author: OXTOBY
Publisher: CENGAGE L
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Draw the organic product(s) of the following reaction.
CH3
CH3
NBS
monosubstitution products
CCl4
You do not have to consider stereochemistry.
Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner.
Separate multiple products using the + sign from the drop-down menu.
Please correct answer and don't use hand rating
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- (B). [8 pts] Draw both the chair conformations of (1R,25)-1-(tert-butyl)-2-butylcyclohexane and circle the more stable conformation. (C). [8 pts] Draw Fischer projections of the all stereoisomeric 2,3-Dichloro butane. Label each of them as erythro/threo/meso as appropriate.arrow_forwardPlease correct answer and don't use hand ratingarrow_forwardIn this reaction, after they add the epoxide, then they add water. Why doesn't adding water to an epoxide produce a 1,2-diol? Wouldn't the water form a bond with one of the carbons on the ring when it opens the ring?arrow_forward
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