Identify the most productive reagent and solvent or combination/sequence of reagents and solvents needed to perform...
For the following reaction sequence, supply the missing intermediate or reagent/solvent, as appropriate Extra Credit: For the following reaction sequence, supply the missing intermediate or reagent/solvent, as appropriate. 1) 2) H", H,O Br DMF Extra Credit: Over the arrow, write in the reagents needed to perform the following transformation. Be specific about the number of equivalents (moles) required for each reagent and about the order of the steps Br
Identify the reagents needed in the following reaction sequence that are represented by the letters A to F: OH Br A B C OH .ک) COOH E onor
Among the mentioned above solvents choose the most polar solvent and write why you chosen this one: a) thyl acetate: b) hexane; c) chloroform; d) diethyl ether
1. (12 pts) Fill in the boxes over each arrow with the letter that corresponds to the reagents needed to perform each step of the multistep sequence shown below. Reagents may be used more than once, or not all. Pay close attention to the numbered carbons in the starting material, and be sure that your answer accounts for the position of these carbons in the final product. 1 3 3 3 2 2 MCPBA CF3SO3H A) HOCH3, DCC, DMAP E)...
Pick the sequence of reagents needed for the following reaction 1. 2. 3. Br Possible reagents: A) CH3CH2CI, AICI: B) CH3COCI, AICI3 C) Br2, FeBr 3 D) H*/H20 E) Zn(Hg), HCI 1. [Select) 2. [Select ] 3. [Select)
COOH COOH OH OH Select reagents from the table to perform this synthesis; only one reagent is required for each step. If the synthesis has fewer than 4 steps, choose (none) for the unneeded steps. Reagents a. CH3CI, AICI: b. Bre, FeBrz c. NaOH; then CO2, H2O; then H307 d. KMnO4, H* e. Cl2, FeCl3 f. NaOH, H20; then SO2(OCH3)2 g. Cl2 h. HNO3, H2SO4 Step 1: Step 2: Step 3: Step 4:
PLEASE HELP 3. Why are alcohols or water an inappropriate solvent for dissolving sodium hydride or potassium amide? Write a detailed mechanism to justify your answer. 5. Starting with acetylene, should reagents that could be used to prepare each of the following: a. 1-butyne b. 2-butyne C. 3-hexyne d. 2-hexyne e. 2-heptyne f. 3-heptyne g. 2-octyne h. 2-pentyne i. 1-hexyne 6. Propose a synthesis for affording the transformation below. 7. Show how one could synthesize each of the following from...
Fill in the boxes over each arrow with the letter that corresponds to the reagents needed to perform each step of the multistep synthesis show below. Reagents may be used more than once, or not at all. Pay close attention to the numbered carbons in the starting material, and be sure that your answer accounts for the position of these carbons in the final product. pts) Fill in the boxes over each arrow with the letter that corresponds to the...
i need help with the prelab questions please Grignard reagent THE GRIGNARD REAGENT-PREPARATION AND REACTION In this experiment, you will prepare a Grignard reagent, phenyl magnesium bromide, from bromobenzene and magnesium metal. The Grignard reagent will then react with methyl benzoate to form triphenylmethanol. Introduction Grignard reagents, such as organomagnesium halides, were discovered in 1910 by French chemist Victor Grignard. The Grignard reaction is one of the most general methods for carbon- carbon bond formation in all of organic chemistry....
O 35. Starting with phthalic anhydride, which other reagents are needed for the Gabriel amine synthesis?: A. NH3, A / KOH, 1-pentyl-Br / H2NNH2 NH2 B. KOH, NH3 / LDA, 1-pentanol / NaOH C. NBS, Br2, A/HCI, pentanamide / NaNO2, HCI D. NH3, HC / NaH, 1-pentyl-CI/ KCN 36. Select the final product for the multi-step sequence indicated below: NHA ACCI Etci NaNO2 pyr. AICI: KOH HCI HBF4 ? BF3 Н. A. B. HO D. CI OH