Last question for tonight. I am told I have the following nreagents in this order: 1 Br2, hv, CBr4, then 2) H2O, then 3) CrO3, then NaH, THF and finally 5). CH3I, THF. The product is 3-methyl-2-butanone. Can't find the right alkane as my starting material.
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Last question for tonight. I am told I have the following nreagents in this order: 1 Br2, hv, CBr4, then 2) H2O, then 3) CrO3, then NaH, THF and finally 5). CH3I, THF. The product is 3-methyl-2-butanone. Can't find the right
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- We have a hydrocarbon, C16H26. The compound has two triple bonds and the acids produced by ozonolysis are CH3(CH2)4CO2H and H2OCCH2CO2H. What is a likely structure for this hydrocarbon?"A research team synthesizes a novel organic compound 'X' with the molecular formula C5H8O2. When 'X' is treated with a deuterated acid (D2O), a single deuterium atom replaces a hydrogen atom, forming compound 'Y' (C5H7DO2). 'X' does not react with 2,4-Dinitrophenylhydrazine (2,4-DNP) but does react with both Tollens' reagent and Benedict's solution, forming a silver mirror and a red precipitate, respectively. Furthermore, 'X' undergoes catalytic hydrogenation over a palladium catalyst, consuming one mole of hydrogen to form a compound 'Z' (C5H10O2). Based on these observations, what is the most likely structure of compound 'X'?" A. Methyl vinyl ketone B. 3-Buten-2-one C. Acetoacetic ester D. 2-Hydroxypent-3-enalDraw structural formulas for the major organic product(s) of the reaction shown below. CN 8 + (CH3)2CHCI AIC13 • You do not have to consider stereochemistry. If no reaction occurs, draw the organic starting material. • Remember to include all of the formal charges on the atoms of any nitro groups. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. Separate multiple products using the + sign from the drop- down menu.