4x. A. Using only methyl-3-methylbutanoate develop a synthetic sequence leading to the compound shown.
using 2-methyl propane and ethyne as your only source of
carbon, purpose a synthetic route to make the following.
9. Using 2-methyl propane following. and ethyne as your only source of carbon propo only source of carbon propose a synthetic route to make the ucing only ethyne methyl halide or Mac
pleqse explain and draw structures! Thank you!
Propose a synthetic route using only ethyne and methyl halide as your only source of carbon (all alkyl halides with 2 or more carbons needed should be synthesized) 10. 11. HO 12.
Propose a synthetic route using only ethyne and methyl halide as your only source of carbon (all alkyl halides with 2 or more carbons needed should be synthesized) 10. 11. HO 12.
mechanism
and 9) Provide the sequence of synthetic steps necessary to convert cyclohexanone into the compound shown CO2Et ise mechanism for the transformation shown below
part a
part b
Outline a synthetic method for the preparation of the compound shown below starting from cyclohexanone. Use any reagents that are needed. You may need to scan/take a picture of your answers and e-mail me your answers. CHLB Target Molecule Outline a synthetic method for the preparation of acetophenone(phenyl methyl ketone) starting from bromobenzene. Use any reagents that are needed.
Propose a synthetic strategy for the following
compound.
Exam 3 vers 14) Propose a synthetic strategy for the following compound. Indicate the following (6 pts total): - step that needs to be done to add desired functional group (ex: alkylation; acylation; etc.) - compound required to add desired functional group (ex: CH3CI, etc.) - show the sequence of reactions - include appropriate ancillary reagents (e.g. - FeCl3, AIC13, H2O, etc.) NO2 CH3 (start from benzene)
find the quotient and reminder using synthetic division 2x^4+5x^3+4x^2+7x+9/x+0.5
1) Using 3-methyl-1-butene as the only source of carbon, and any other reagents, outline a synthesis for each compound a) 3 b) c)
The correct IUPAC name for the compound shown below is: CH3 O2-bromo-6-methyl-3-heptyne O2-bromo-6-methyl-3-heptane O 6-methyl-2-bromo-3-heptyne O2-bromo-6-methyl-3-heptene O 6-bromo-2-methyl-4-heptyne
Devise an efficient synthetic sequence for the formation of meso-3,4-hexanediol, using any and as many two carbon compounds as your only sources of carbon. Be sure to include any necessary reagents and solvents.
Several reagents and several organic structures are shown below.
Construct a multistep synthetic route from the reactant
2-methyl-1-butene to the product 3-bromo-2-methyl-2-butanol by
dragging the appropriate pieces into the bins. Note that each bin
will hold only one item, and not every given reagent or structure
will be used.