Place the best reagent and conditions in the bins for each of the following reactions. (Stoichiometry...
In each reaction box, place the best reagent and conditions from the list below. In each reaction box, place the best reagent and conditions from the list below. Only one of the reagents can react with the very unreactive cyclopentane. A radical intermediate is involved. PCC stands for pyridinium chlorochromate. It oxidizes a primary alcohol to an aldehyde or a secondary alcohol to a ketone.
In each reaction box, place the best reagent or reactant from the list below. Stoichiometry is omitted.
In each reaction box, place the best reagent and conditions from the list below. A reagent may be used more than once.) Alkylating with ethyl bromide in steps 2 and 4 will lengthen the alkyne by two carbons at both ends but will not introduce the primary alcohol functional group.
?? Three reactions between a Grignard reagent and a carbonyl compound are given below. Draw the main organic product for each reaction and indicate if H+ or H- is needed to complete each reaction. (The starting material structures are provided in the answer fields as a starting point for your drawings.) Ketone reaction Ester reaction Acyl halide reaction Above, keep in mind that two equivalents of the Grignard reagent are utilized. What is the intermediate product resulting from the addition...
In each reaction box, place the best reagent or reactant from the list below. Stoichiometry is omitted. Reactant A Reagent B ,then H3O 2) Reagent c PCC PBr3 ethyl acetate acetone NaBHa ethylene oxide Mg in Et20 NaH C3H7Br 1) Reagent D 2) Reactant E 3) H3o* OH
In each reaction box, place the best reagent or reactant from the list supplied. Stoichiometry is omitted. 1. Reagent B, then H30* 1. Reagent D OH C Reactant A C3H7Br 2. Reagent C 2. Reagent E 3. H30+ Answer Bank PCC Mg in Etz NaH NaBH4 PB13 acetone ethylene oxide EtOAc
In each reaction box, place the best reagent and conditions from the list below. In each reaction box, place the best reagent and conditions from the list below. Your reagent for the third step is incorrect. In this step an alcohol is converted to an aldehyde.
In each reaction box, place the best reagent and conditions from the list below. In each reaction box, place the best reagent and conditions from the list below. In each reaction box, place the best reagent and conditions from the list below. Your reagent for the first step is incorrect. This reaction involved a double elimination of HBr to form an alkyne. Which reagent is a strong base capable of carrying out this reaction ?
In each reaction box, place the best reagent and conditions from the list. Answer Bank acetate ion acetone CH, MgBr (excess) H,0,H,O, heat acetic acid NaBH acetyl chloride CH, OH, HO* (cat.) H2O LÃAll | (CHỊ),CHMgBr (excess) NaNH, CH, CH,MgBr (excess) HR UN SEC Question 2 of 11 > Analyze both reactions and indicate whether the equilibrium tends to favor the reactants or the products. > - İri. - immi. 0 Select the true statement(s). O Reactions A and B...
In each reaction box, place the best reagent and conditions from the list below. In each reaction box, place the best reagent and conditions from the list below. 1) 2) 3) 4) но. но он t-butyldimethylsilyl chloride triethylamine NaNH2 Mg, Et20H3OF KMnO4acetyl chlorideCrO3, H2SO4 H2, Pt CO2 PBr3, pyridine NaBH4 NaCN