Show how to carry out the following synthesis, using any 3 carbon species as your only carbon sources. You may use any additional reagents necessary. Pay attention to the overall efficiency of your synthesis. 210 6. acetone any 3 carbon source 3-propylhexane-2,4-dione + I have drawn my synthesis on my answer sheet [Answer: yes or no] How many steps are in your synthesis? Give the number of steps in the box below. [Answer: 1, 2, 3, 4, etc.]

Show the reagents for the conversion below: COOH OH NO2

Shown below is a proposed synthesis of the target molecule, starting with benzene: Part 1 Reagent(s) H₂N Last Step Reagent(s) Ph Ph Part 2 Reagent(s) The transformations above can be performed with some reagent or combination of the reagents listed below. Give the necessary reagents for each part in the correct order, as a string of letters (without spaces or punctuation, such as "EBF"). If there is more than one correct solution, provide just one answer. A. ia + AICI 3 B. CI D. Mg i 2) H3O+ C. 1) Fe, H3O+; 2) NaOH H E. Br2, AICI 3 H F. NaBH3CN, H+ G. NaN 3 H. PCC or DMP J. NaNH2, NH3 K. HNO3, H2SO4 Part 1 Reagent(s): Part 2 Reagent(s): Last Step Reagent(s): I. 1) LiAlH4; 2) H₂O L. NaBH4, MeOH

You are trying to determine whether the following organic reaction can be done in a single synthesis step. If so, add any missing reagents or conditions in the drawing area below. If it isn't possible to do this reaction in a single synthesis step, check the box below the drawing area instead. 口 OH : + T X Cl