3) Draw a complete, step-wise curved arrow mechanism for the transformation shown below. You may use H-B for any Broensted acid and B- for any Broensted base. (6 points) AlCl3, CICH 3
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- What is shown below is an interesting way of making lactone B from lactone A. The reaction takes place when A is treated with sodium hydride, a strong base, which deprotonates the OH group. Draw a curved arrow mechanism which explains how B is formed. The reaction takes place in multiple steps. Show all curved arrows, relevant lone pairs, and formal charges. (7 p) OH H = A Br NaH H [strong base] H B[4.6 pts] Draw the mechanism for the reaction listed below. لي acetone benzaldehyde NaOH1. (10 points). Draw a stepwise detailed mechanism for the following reaction showing all the substitution and the elimination products formed. Label the type of the mechanism (SN1, SN2, E1 or E2). Show stereochemistry when applicable. Br CH3CH2OH H₂O 2. (10 points) 0 Br CH3O Na DMSO Draw the detailed mechanism showing ALL possible products formed including stereochemistry and Label mechanism as SN1, SN2, E1 or E2. Show stereochemistry when applicable.
- For the following reaction draw the flipped chair and draw the elimination product of the reaction. No mechanism required.1. Please name the following compounds. (9 points) Br CI Br Br 2. Please draw the major product(s) of the following reaction and show the mechanism. Is there a reason why one stereochemistry is preferred over the other for this reaction? (9 points)What is the most stable carbocation
- 1. (10 points) Complete the reaction scheme below. Show all reagents and intermediates. No reaction is a possible answer. Do not neglect stereochemistry. NaCN DIBAL Br A "OCH3 (sodium cyanide)Draw a curved arrow mechanism for the substitution reaction that will occur with the alkyl halide and nucleophile below, adding steps as necessary. Be sure to include all nonbonding electrons and all nonzero formal charges, and show all species that react or are formed in this reaction.4. (a) Draw all possible stereoisomers of HOCH2CHOHCHOHCH2OH using zig zag format. Calculate how many possible there are first.(b) Circle two that will have identical water solubilities. (c) Place a box around two that will have different water solubilities. Assign R/S configuration to each stereogenic center. Total # of possible stereoisomers:
- (a) Add curved arrows for each step to show how A is converted to the epoxy ketone C. (b) Classify the conversion of A to C as a substitution, elimination, or addition. (c) Draw one additional resonance structure for B.Draw a curved arrow mechanism for the reaction. You can assume that all reactants and products are shown. Add/Remove step CN :C=N:help please answer in text form with proper workings and explanation for each and every part and steps with concept and introduction no AI no copy paste remember answer must be in proper format with all working