Shown below is the synthesis of N,N-dimethyl-2-methylhexanamide
from diethyl malonate. Fill in the best reagents to achieve this
synthetic transformation. Note: If one or more reagents are
incorrectly placed, a single red X will appear on the top left.
Shown below is the synthesis of N,N-dimethyl-2-methylhexanamide from diethyl malonate. Fill in the best reagents to...
Shown below is the synthesis of N, N-dimethyl-2-methylhexanamide from diethyl malonate. Fill in the best reagents to achieve this synthetic transformation.
Fill in the appropriate reagents to achieve the synthetic transformation shown below. Note: If one or more reagents are incorrectly placed, a single red X will appear on the top left. Map Sapling Learning macmilan learning Fill in the appropriate reaets to achieve the synthetic transformation shown below. Note: If one or more reagents are incorrectly placed, a single re X appear on the top left 2. 3. 4. 5. Mg, ether NaH Br(CH2)2CH3 CH3(CH2ho NaOH CH3(CH2MgBr acetone H30*
Label the reaction with the reagents necessary to facilitate the transformation below. Note that if one or more reagents are incorrectly placed, a single red X will appear on the top left.
Select the missing reagents needed to convert each molecule into the next one pictured in the synthetic scheme below. Note: If one or more reagents are incorrectly placed, a single red X will appear on the top left. Select the missing reagents needed to convert each molecule into the next one pictured in the synthetic scheme below. Note: Ifone or more reagents are incorrectly placed, a single red X will appear on the top left. 1. acetone Brz. CH3CH2OH H30...
In each reaction box, place the best reagent and conditions from the list below. Note: If one or more reagents are incorrectly placed, a single red X will appear on the top left. он 2. 3. он он
Starting with cyclohexene, propose a reasonable synthesis of the cyclohexene derivative below. If one or more reagents are incorrectly placed, a single red X will appear on the top left.
Drag the labels to identify the appropriate reagents for each reaction below. Each label is associated with the arrow adjacent to it. The direction of the arrow is important! Note: If one or more reagents are incorrectly placed, a single red X will appear on the top left. Drag the labels to identify the appropriate reagents for each reaction below. Each label is associated with the arrow adjacent to it. The direction of the arrow is important! Note: If one...
Propose a synthesis of the following derivative of diethyl malonate using reagents from the choices provided below. (From the choices provided, list the reagent(s) in order that will accomplish this transformation. No more than 4 steps are required. List your answer as a single letter (single-step transformation) or a series of letters (multi-step transformation) with no commas separating them.) Reagents available a. Eto Na g. CH2=CHCH=CHCH,Br b. CH3 CH2Br c. CH3 CH, CH, CH(CH3)Br d. (CH3)2 CHCH, CH,Br e. CH3...
In each reaction box, place the best reagent and conditions from the list below. There is more than one possible route. Note: If one or more reagents are incorrectly placed, a single red X will appear on the top left. CH3CHO, 2H2O CH2CH2CH2CHO, 2H2O CH3(CH2)2MgBr, H2O CH3MgBr, H2O CH3(CH2)2OH Mg CH3Br PCC HOCH2CH2OH, H+ H3O+
8. Give a synthesis of the compound shown starting from either diethyl malonate (DEM) or ethyl acetoacetate (EAA) shown in the box below. Give all reagents necessary. State clearly whether your starting compound is DEM or EAA. You do not need to draw the intermediate steps. 17 pts] Eto Et Hoce DEM ΕΑΑ. 9. Draw the uncharged product of this synthetic sequence. [4 pts] 1. KOH OCH 3. NaOH(aq) excess 10. By how much will the mass of this compound...