Physical Properties of Alkyl Halides (polarity, polarizability, high density) Explain regioselectivity of bromination vs chlorination Special reactivity and Resonance structure of Allylic and benzylic position. Stability of radicals (primary vs

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Usually at the 2- or 3- position, Thiophene undergoes electrophilic aromatic substitution. Draw the intermediates and all resonance structures for the reaction at each position, and then decide what position should be more reactive depending on your intermediates.

3) Provide the structure of the major organic product in the following reaction. CH3 4) Classify the compound below as aromatic, anti- aromatic, or non-aromatic. H 5) Classify the compound below as aromatic antiaromatic, or nonaromatic. Assume planarity of the TT network. B N 6) Provide the structure of the major mononitration product of the compound below or write "no reaction" if you think so. (hint: methoxy group is a stronger EDG than phenyl group) OCH 3

Please don't provide handwriting solution

Identify the major product of the following: C6H5MgBr then H3O+ hydrazine, H₂NNH₂ KOH PCC,CH₂Cl₂ LiAlH4 then water H Benedict's solution H -CH₂OH Choose... Choose... 1,1-diphenylethanol benzoic acid 1-phenylethanmine propylbenzene cyclopentanaldehyde No reaction 1-phenylethanol propanoic acid propan-1-ol cyclopentanecarbaldehyde OnG09... Choose... Choose... 4 <

In the following nucleophilic substitution reaction, does the top or bottom have the higher reaction rate. Why?

Which alkene is LEAST reactive in acid-catalyzed hydration? all have equal reactivity А. В. c. D. Е.

question about reagents

Rank the following radicals in order of increasing stability.