What alkyl bromide would give the following as the predominant product upon treatment with KO-t-Bu / t-BuOH? Be sure to show stereochemistry.
What alkyl bromide would give the following as the predominant product upon treatment with KO-t-Bu /...
Draw the organic product(s) of the following reaction. KO-t-Bu/t-BuOH CEC-H If no reaction occurs, draw the organic starting material Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. Separate multiple products using the +sign from the drop-down menu. Include counter-ions, e.g., Na", I, in your submission, but draw them in their own separate sketcher.
please explain the work 5. Predict the major product for the following elimination reaction. Make sure that you draw any relevant chair conformers to support your answer. KOt-Bu H3C CH3 t-BuOH CH3 6. Draw a cycloalkyl bromide with molecular formula C7H13Br that would give exclusively the following alkene under E2 reaction conditions. Use wedges and/or hashes to show the relative stereochemical relationships between groups, and support your answer with a relevant chair structure. CH3 KOt-Bu t-BuOH
The following alkyl bromide can react with NaF via an Sn1 mechanism. Draw the mechanism and product(s) of this reaction. Be sure to pay attention to stereochemistry, if applicable.
7) The following alkyl bromide can react with NaF via an Syl mechanism. Draw the mechanism and product(s) of this reaction. Be sure to pay attention to stereochemistry, if applicable. NaF
The following alkyl bromide can give several elimination products Br Base Me Me (a) Give the expected elimination products (b) For each product, show how selective deuteration could reduce its yield relative to the other E2 products (i.e., show one deuterated derivative for each expected product)
Show the alkyl bromide and alcohol used to make methyl t-butyl ether using the Williamson ether synthesis to the right of the retrosynthetic arrow. Mapoob a) Show the alkyl bromide and alcohol used to make methyl t-butyl ether using the Williamson ether synthesis to the right of the retrosynthetic arrow. alcohol alkyl bromide click to edit CHa H3 H3 b) Complete the general mechanism by adding curved arrows and drawing the final organic product. (Note that R is an abbreviation...
Which starting material would give rise to the following product exclusively upon treatment with Oz/DMS? 03. DMS ismul HC CH (A) CH CH3
Pleaseee only answer if you know the right answer.. I will rate 5. Predict the major product for the following elimination reaction. Make sure that you draw any relevant chair conformers to support your answer. Ts KOt-Bu H3C "ICH3 t-BuOH CH3 6. Draw a cycloalkyl bromide with molecular formula C7H13Br that would give exclusively the following alkene under E2 reaction conditions. Use wedges and/or hashes to show the relative stereochemical relationships between groups, and support your answer with a relevant...
please explain the work 3. Predict the major product for the following elimination reaction. Make sure that you draw any relevant Newman projections (looking down the C3-C4 bond) to support your answer. KOt-Bu t-BuOH 4. Draw a dibromide with molecular formula C14H12Br2 that would give exclusively the following alkene under E2 reaction conditions. Use wedges and/or hashes to show the relative stereochemical relationships between groups, and support your answer with a relevant Newman projection. KOt-Bu t-BuOH
t-Bu What product(s) would you expect to obtain from acid-catalyzed hydrolysis of the single epoxide stereoisomer above? - Use the wedge/hash bond tools to indicate stereochemistry where it exists. Keep the alkyl group in the same orientation as in the figure. . If the reaction produces a racemie mixture, draw both stereoisomers. Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner • Separate multiple products using the + sign from the drop...