Show how to carry out the following transformation. Show all reagents and all molecules synthesized along the way. You do not have to use curved arrows. • You are not allowed to use NBS/light or Br2/light. • You MUST use SOCI2/pyr. ?
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- Show how to carry out the following transformation. Show all reagents and all molecules synthesized along the way. You do not have to use curved arrows. You are not allowed to use NBS/light or Br2/light. You MUST use SOCl2/pyr. for this drawingShow how to carry out the following transformation. Show all reagents and all molecules synthesized along the way. You do not have to use curved arrows. • You are not allowed to use NBS/light or Br2/light. • You MUST use SOCI2/pyr.´. HOPropose a multi-step synthesis of the target molecule shown at the right, using the starting materials on the left and any other reagents you need. Show the reagents needed for each step and the product of each step. You will need 4 reaction arrows.
- Propose an efficient synthesis for the follwoing transformation. You may use any reagent you need. You do need to show mechanism and products for each individual reaction.Identify reagents that can be used to complete the following transformation. o OH OH O BH3-THF O 1) LiAlH4, 2) H30* O NaOH, Please do it correctly and don't copy or paste from anywhere otherwise I will report you and you gonna dismissed.Complete the following reactions in sequential order. Show the product after each step and put a box around the final product. (Show intermediate structure after each reagent)
- Complete the following reaction sequences by drawing the major products or the reagents necessary to make them. Be sure to include stereochemistry when appropriate. Please answer fast I give you upvotePlease propose reagents that complete the following transformation, showing all intermediates.Draw a mechanism for the following transformation. For the mechanism, draw the curved arrows as needed. Include lone pairs and charges in your answer. Do not draw out any hydrogen explicitly in your products. Do not use abbreviations such as Me or Ph. CH3CI AICI3 18.49d1 Draw step 1 of the mechanism. CI H,C-CI + Al, CI Edit Drawing
- Provide a reagent that will complete the transformations.The following molecules are subject to substitution (SN1 or SN2) reaction conditions. a) Identify if the leaving group (-Br) is attached to a 3°, 2°, 1°, or methyl Carbon. b) Rank the molecule with respect to their SN1 reactivity, with 1 being the fastest and 4 being the slowest. c) Rank the molecule with respect to their SN2 reactivity, with 1 being the fastest and 4 being the slowest. Br Br CH3B Br a. type of Carbon on C-Br b. SN1 reactivity (1 fastest, 4 slowest) c. SN2 reactivity (1 fastest, 4 slowest)Give a mechanism for the following reaction. Indicate electron flow with arrows. Show the structures of intermediates. Be sure your mechanism explains the observed stereochemistry (syn or anti) and regiochemistry (Markovnikov or anti-Markovnikov).