How to get from the right one to the left one. You can use any reagents.
How to get from the right one to the left one. You can use any reagents....
From the table of available reagents select the one(s) you would use to convert butanoic acid to each of the following products: (Use the minimum number of steps; from one to six are required. List reagents by letter in the order that they are used; example: fa. NOTE: Assume that a normal aqueous (or mild acid) workup follows each reaction; you do not need to add reagents for the workup.) Reagents Available a. benzene/AlCl3 d. H2O, H2SO4 g. LiAlH b....
Organic Chemistry. How do you go from beginning(left) to the end(right)? Reagents and intermediate materials to target product molecule.
Organic Chemistry. How do you go from beginning(left) to the end(right)? Reagents and intermediate materials to target product molecule.
Organic Chemistry. How do you go from beginning(left) to the end(right)? Reagents and intermediate materials to target product molecule. 1 / Br Br
Example #2 Synthesis the molecule on the right from the one the left. Give reagents, conditions and intermediate molecules in each step. ?????? Br
[References] From the table of available reagents select the one(s) you would use to convert cyclohexanone to the following compound: CH2CH2CO2H Use the minimum number of steps: from one to five are required. List reagents by letter in the order that they are used; example: fa. Reagents Available a. BH3, THF; followed by H2O2, OH g. Nat -CH(CO2C2H5) (from CH2(CO2C2H5)2 + Nat -OC2H5) b. Br2, CH3CO2H h. PBr3 c. HCN, KCN i. PhCH Br d. H307, heat j. Ph3P+- CH2...
lPropose a synthesis of each. You may use any needed inorganic reagents and solvents. a) (CH3)3CCl from (CH3)3COH b) trans-1,2-cyclohexanediol from bromocyclohex ane
How would you synthesize the following compound from acetylene and reagents in the table? Choose the most efficient route. Specify reagents using letters from the table, first reagent on the left. Example: ab H H CH3CH2CH2 CH2CH3 a. Br2 b. CH3CH I Reagents available d. CH3 CH2CH2CH2Br g. KOH/ ethanol e. Hy / Lindlar's catalyst | h. NaNH / NH3 f. 1. BHz in THF 2. H2O2 in NaOH c. CH3 CH, CH,Br Reagents (in order of use) are Submit...
Can you explain how to approach this problem and then the steps you use to get to the solution as well? 4. Convert the following structures: to a condensed structure: -OH to a skeletal structure: (CH3)-C(CHỊ) CHO to a skeletal structure : CHỊCHÚC(CH3)-CHÚCONH,
Show how the following compound could be prepared from ethyne. You may use any necessary reagents. You must show all stable intermediates formed along the way and all necessary reagents used (10 points). OS multiple steps! Hinh .