Consider the following reaction: OH Н4С H,SO CH3 + ОН A Show the complete mechanism for...
^ the top has been answered already Consider the following reaction: OH Н4С H,SO CH3 + ОН A Show the complete mechanism for the following transformations. Make sure to show all arrows depicting the movement of electrons. The above reaction (using acid and heat) causes a number of unwanted side products to form (a big mess). Propose a better synthesis for the product using the same starting materials. Show the reagents and intermediate steps to complete the synthesis: ОН. HzC...
Consider the following reaction: OH HC H.SO CH, + ОН Δ Show the complete mechanism for the following transformations. Make sure to show all arrows depicting the movement of electrons. The above reaction (using acid and heat) causes a number of unwanted side products to form (a big mess). Propose a better synthesis for the product using the same starting materials. Show the reagents and intermediate steps to complete the synthesis: OH H3C- ??? + CH3 OH X steps Propose...
Show the complete mechanism for the following transformations. Make sure to show all arrows depicting the movement of electrons. ОН H3C- х + H2SO4 Д -OH
Show the following mechanism with all steps and make sure to draw all arrows depicting the movement of electrons. CH3 с из СИ KMnO4, 60 -CH3 heat
3. Write a mechanism for the following reaction. Include formal charges and curved arrows to show the movement of electrons in all steps. (6 pts) O CHỊCH CH3CH ОН H,0 CH3CH,MgBr S ether H3O+ OH CH3C=CH ether CH3C=CCHCH,
Question 3 Draw the mechanism for the following transformations: Нас снз CH3 H-SO Hс Он Question 4: 1) Hg(OAc) H,o 2) NaBH Нас- CHy Н,с сн, Question 5: Predict the product(s) of the following reaction: 1) BH, THF 2) H2O2, NaOH CH2 H,с Question 6: Predict the products of each of the following reactions: CH3 Hас- На Ni - CH3
x H R OH ОН R this method does not work Fischer esterification cannot be used to prepare tert-butyl esters. Draw curved arrows to show the movement of electrons in this step of the reaction mechanism. Arrow-pushing Instructions :0: + :OH ox H-OH ox H20 R R
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:
Complete the mechanism for the following dehydration reaction by adding formal charges and arrows to indicate the movement of electrons. Write the overall equation at the bottom. O: H-Cl : CH3 CI: CH Нас 2) CH CH3 CH3 H3C H3c 3) CI overall equation:
3. Propose a reasonable mechanism for the following transformations. OH [H,80] НО 4. Predict the product of the following transformation by drawing the mechanism of the reaction. Н4С H H20 CH₂CH2 CHA Br2