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OH - draw the mechanism: ix CH3CH20H - draw the synthetic pathway: HO Starting from cycle...
OH - draw the mechanism: ix CH3CH20H - draw the synthetic pathway: HO Starting from cycle penty! bromide and [diethyl_malonate or ethyl acetoacetate] (os appropriate) draw the synthetic pathway! OCH2 CH3 -CH3
22. Starting with 1-hexene, which synthetic pathway below gives 2-cyanohexane? CN ? (a) HSO. (cat), H20; then NaCN (b) HBr/peroxide; then NaCN (c) HBr; then NaCN (d) Bry/H_O; then NaCN 23. [9 pts) Write out a complete mechanism for the following transformation: Br CH,CH,OH You 24. (20 pts] Draw the major expected organic product(s) for each of the following reactions. Be sure to indicate stereochemistry when needed. 1) TSCI, Pyr 2) NaB Br HS 1) SOCI. pyridine 2) NaSH OH...
• Provide the step-by-step synthesis route/pathway (not mechanism) from the below starting material to the desired final product. (4 points) OH
HO OH ОН Ethylene oxide is the starting material for the synthesis of 1,4-dioxepane. Draw curved arrows to show the movement of electrons in this step of the reaction mechanism. Arrow-pushing Instructions :o: Hö: H-OH :0:
Draw a mechanism for the following reaction: HT HO. OH Draw all missing reactants and/or products in the appropriate boxes by placing atoms on the canvas and connecting them with bonds. Add charges w Electron-flow arrows should start on the electron(s) of an atom or a bond and should end on an atom, bond, or location where a new bond should be c LH: H + с N OCO +'1 0 +f H+ O HO: N OH S CI Br
Help with part e please! 3. Consider the following Sw1 reaction. CHg CH,-Ẻ-CHCH + HO --- ne bo pomem e no — a potom os CHE CH-C-CHÚCH + I" OH a. Draw a mechanism for this reaction using curved arrows. b. Draw an energy diagram. Label the axes, starting material, product, E, and . Assume that the starting material and product are equal in energy. c. Draw the structure of any transition states. d. What is the rate equation for...
1. For each reaction below, draw the reaction mechanism for the rate determining step. On the starting structures, draw all appropriate arrows to indicate the flow of electrons. Fill in the box above the arrows with the reaction mechanism as SN1 or SN2. Draw the first key transition state and product(s). Use dotted lines to indicate bonds that are in the process of being broken or made. Write all formal charges. н н * HC CI: Transition State H HD...
Look up and draw the mechanism for the addition of Br2 to double bonds. Reference the source from which you acquired the mechanism. Give the IUPAC name of the major product in the above-mentioned reaction. Draw the major product of obtained in the addition of Br2 to stilbene. Is this isomer chiral? What would be the optical rotation if this sample was placed in a polarimeter? Would a student obtain the same product if you started with cis-stilbene instead of...