Fill in the box with either the reagents/conditions/ product (whatever is required) to complete the given synthesis scheme.
Fill in the box with either the reagents/conditions/ product (whatever is required) to complete the given...
Fill in appropriate reagents and conditions to complete the reactions in the scheme below. If you need multiple steps for one transformation, make sure to number them appropriately (and only one step per box please).
1. (6 pts) Fill in the blanks to complete the reaction scheme. If multiple products/reagents are possible, choose one that will allow the rest of the synthesis to occur. If multiple stereoisomers form, only draw one. NaOH mCPBA ''Br KOtBu 1) BH3, THE 2) H2O2, NaOH
synthesis questions, please explain! 13. (10 pts.) Fill in the missing reagents or product in the following synthesis HO H2SO4 PCC CH2CH2 Diethyl ether 2. H30* 14. (10 pts.) Fill in the missing products. MOBI Diethyl ether n mCPBA mCPBA NaH
Solve the missing steps along with reagents/ reaction conditions required to synthesize the given final product (not necessarily 3 steps, just indication that it is multistep) ت . . . ت مادH HC
Complete the following reactions with the miss reagents(s) or major product(s). Br Hint: This Scheme involves Williamson Synthesis Xorph Ph HI (excess) OH
Please explain!! Thank you!! I will rate! Fill in either the missing product or reagents (over the arrow) CH H3C CH2 KmN04 H2C1 CH3 Lindlars H2C OH H3c
2. Fill in the missing reactants, reagents & conditions, or products. Don't worry about stereochemistry, unless indicated. 1. LDA, -78c OCH then H3o 0 CO Et H3o C10H100 CH NaOEt (aq) 0 0 NaOH (aq) NaOEt (aq) 0
Any help is greatly appreciated!!! 3) Fill in the boxes with the missing product or reagents needed in the following reactions (2 pts each) Pyridine SH Pyridine SOCI2 Pyridine Pyridine 4) Fill in the boxes with the missing product or reagents needed in the following reactions (6 pts total) MgBr KCN
(10 pts) Fill in the missing intermediates (two), final product, and reagents (two) in the llowing multistep synthesis. Br X OH -- NH 에 CH,Br 6) (5 pts) Write out the 3-step arrow pushing mechanism showing how cyclopentanol is dehydrated to make cyclopentene: он conc. H,SO + HO heat
From the table of reagents shown below, show how you synthesize the product from the given reactant. Reagents available (Enter the letter(s) of the reagent(s) needed in the box, in the order that they must be used. No more than two steps are required to perform the synthesis. Note that a retrosynthetic arrow is used, and therefore the reactant is shown on the right.) Answer: