Propose a structure for an alkyl halide that generates only (Z)-3-methyl-2-phenylpent-2-ene upon E2 elimination with NaOH. Include: The curved arrows to show the mechanism of the transformation The IUPAC name of the proposed starting material (including stereocenters) NaOH alkyl halide (Z)-3-methyl-2-phenylpent-2-ene IUPAC name of alkyl halide:

Choose one (and only one) of the reactions below and draw the complete mechanism for the major product(s) only, including the formation of the electrophile. You must also include all of the proper resonance structures for any intermediate species, but not for the starting material. Be sure to also include all arrows, charges, electrons, and any other mechanistic aspects discussed in lecture or within your textbook. Upload your answer (using any reasonable file format) within this question. Reaction I HO 1. AICI3 H 2. H-О H3C CI Reaction II H,SO4 NO2 Reaction III FeCl3 + Cl2 SO3H

Give detailed mechanism Solution with explanation needed. don't give Handwritten answer. Don't give Ai generated solution

Show the mechanism for this reaction of alkynes