Migratory aptitude is defined as the relative ability of a group to migrate in a rearrangement reaction. Considering your answer to question #2 above, which group do you expect to have "greater migratory aptitude" (in other words, which group is more likely to migrate) in the following compound, benzene, or methoxy-substituted benzene? Draw the product of the reaction after the group with "greater migratory aptitude" migrates. ОН OH H3CO OCH3

Draw the structure of the major organic product of the reaction below. CH₂ + CHCI 3 KOH Use the wedge/hash bond tools to indicate stereochemistry where it exists. Show stereochemistry in a meso compound. If the reaction produces a racemic mixture, just draw one stereoisomer. O. #[ ] در ? ChemDoodleⓇ

Draw the most stable resonance form for the intermediate in the following electrophilic substitution reaction. CH3 CH3 H3PO4 HO, + H3C CH3 HO HO First stage in synthesis of the epoxy and polycarbonate ingredient bisphenol-A You do not have to consider stereochemistry. Include all valence lone pairs in your answer. In cases where there is more than one answer, just draw one.

In which of the following compounds aromatic electrophilic substitution takes place at ortho and/or para position? CH₂-B(OH)2 CH-COCOCH3 CH-CH CH-NO₂

10 16 The major product of the given reaction has the molecular formula C₁0H₁603. Draw its structure in the most stable tautomeric form. Select Draw Rings More Erase C H O ful 1. NaOCH₂CH3 2. H3O+ CH3CH₂OH 2 Q

A benzene ring alters the reactivity of a neighboring group in the so-called “benzylic” position, similarly to how a double bond alters the reactivity of groups in the “allylic” position. Benzylic cations, anions, and radicals are all more stable than simple alkyl intermediates. a) Use resonance structures to show the delocalization of the positive charge, negative charge, and unpaired electron of the benzyl cation, anion, and radical.

Predict the products of this organic reaction: CH3 O || CH3 CH–C−NH—CH3 + NaOH A No Reaction ? Specifically, in the drawing area below draw the structure of the product, or products, of this reaction. If there's more than one product, draw them in any arrangement you like, so long as they aren't touching. If there aren't any products because this reaction won't happen, check the No reaction box under the drawing area. Click anywhere to draw the first atom of your structure. X :0 Ć

Draw the structure of the starting material needed to make 2-methylhept-3-yne using sodium amide in liquid ammonia, followed by 1-bromopropane. The starting hydrocarbon must have no more than five carbons 1) NaNH2, NH3() NaBr + 2) CHзCH2CH2Br

a) b) C) Show the steps necessary, in order, to make each of the following compounds. Start with benzene, and use only reactions we studied this semester. O 10₂ NO₂ -ECH₂CH3 o Br

What is/are the product(s) of the following reaction? Assume the reaction can yield some product(s). CH3CH₂OH + CH₂CH₂ CH₂CH₂OH CH3CH₂CH₂CH₂OCH₂CH₂CH₂CH3 CH3CH₂OCH₂CH₂CH₂CH3 CH3CH₂OCH₂CH3 H3O+ All of the above.