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- In an SN1 reaction, what are the Stereochemistry Consequences: (Retained, Inverted, Lost, Converted)? please be specific. Electrophile-What are the characteristics of a good electrophile for S N1? Alkyl GroupLeaving Group I'm not sure what is meant by alkyl groups and leaving groups in this question. Thank you.You react an unknown aldehyde (substitutent group marked with an "x") with a ketone and get the product on the right (substitutent group still unknown). HNMR data for the product is shown below. Which of these 3 aldehydes is the reactant that was used? sorry the HNMR looks rough, this was the last question on my final and I am still kinda reeling from it.Hi! Could someone help me with these practice problems? I'm having trouble understanding the concepts. First I have to draw the perspective diagrams with dashes and wedges for the major products of the reactions. Then, add an enantiomer where its appropriate. Lastly, note the stereochemistry of the process (syn, anti or none). Thanks so much!
- 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?Hello, could someone help me with this practice problem? thx in advance (: For the major product of this reaction, draw the perspective diagram of the major products. The mechanism isn't necessary, just the products. If appropriate, add an enantiomer where required. Lastly, state the stereochemistry of the process (syn, anti or none).O chem - please break down each step as much as possible, draw all possible products and consider stereochemistry
- Please answer this NEATLY, COMPLETELY, and CORRECTLY for an UPVOTE. What is the product of the reaction below?show all important steps of rxn. (3S,4R)-2-bromo-3-propyl-2- phenylpentane in ch3OH. label arrow, intermediates, and all potential priductsI was wondering if this is correct? Will there be 6 products or are they the same products? Also is the major correct?
- Working Backwards Tutorial. a. First, identify the reactions taking place. Look at the reagent over the arrows. What is the reaction used for? Does it have SN1 or SN2 conditions? b. Now look at the big molecule. Based on your answers to A, circle any portion of the molecule you suspect reacted under these conditions. Is it a stereocenter? c.Based on your answers to A and B, what will be the stereochemical outcome of this reaction?Do the reactions below proceed in good yield from left to right as shown? Please fill in Yes or Noneed all 4 parts along with reaction names in detail don't copy or else I will downvote