c. In reaction B, a second isomeric product is expected to be formed in roughly equal amounts to the product shown. Draw that second product, and label any stereocenters as (R) or (S).
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answer part c for me please
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- Draw the (pericyclic) reaction (reaction 1), including all mechanistic steps, that lead from the starting materials to the intermediate product. Show all isomers that can be formed and provide an explanation as to why that is. Determine the configuration of all chiral centers. I included the molecule, the retrosynthesis of the molecule, and reaction 1 to help solve this question.o chem - please show stereochemistry and break down each step as much as possibledo not fully undsertand the slide,need further explanation. what does it means by the additive effect of two group?which two group ??why OH is a more powerful activator than CH3? meta rarely take please because it is too hindered?why too hindered?Too hindered in EAS or which reaction?why??I am confused.
- 1.Draw the product, please shows step by step in details 2.Explain if (CH3)2CH in this reaction can attach in ortho positon in Friedel Craft Alkylation?? why or why not???The following compound readily eliminates CO; to form a conjugated six membered ring. (a) Complete the reaction with drawing the possible structure and (b) explain why this reaction goes steadily.Consider the following alkyl halides: - may react with NaI to give JKL? - an alkyl iodide that will give SN1 and E1 product? - has the highest boiling point? - most likely to give retention and inversion products in SN1 reaction? - most likely to give rearrangement product in SN1?
- #6). Second picture shows instructions on how the arrows must be shown as.The molecules below react in a displacement reaction. Determine the products) and assign configuration (R/S) to any stereogenic centers in the product. The Cahn-Ingold - Prelog rules can be used to assign priority to the four different groups on a stereogenic center.O chem - please break down each step as much as possible, draw all possible products and consider stereochemistry
- Please help with the following ochem mechanisms.... 1. Provide the stepwise mechanisms for the following reactions (see attached picture)For the reaction scheme below: (a) Suggest a reagent X that could be used to accomplish the first step. (b) Draw the curly arrow mechanism for the second step in the scheme.a. First, identify the reactions taking place. Look at the reagents over the arrows. What is the first reaction used for? Does the second reaction use SN1 or SN2 conditions? b. Now look at the big molecule. Based on your answers to B, circle any portion of the molecule you suspect will react under these conditions. Is it a stereocenter? c. Based on your answers to B and C, what will be the stereochemical outcome of this reaction?