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- Finished A-C need help with the remaining D-IPropose a short synthesis f or ONE of the following molecules. You can start with acetylene, and alkyl halides from 1-4 carbons in length. You can also use an reagents you wish. a) Hexan-3-one (CH3CH2COCH2CH2CH3)Using any necessary organic and inorganic reagents, show how you can carry out the chemical conversions shown below. Please answer parts a, and b.
- The central carbon atom of an allene is a member of two double bonds, and ithas an interesting orbital arrangement that holds the two ends of the molecule at rightangles to each other.(a) Draw an orbital diagram of allene, showing why the two ends are perpendicular.(b) Draw the two enantiomers of penta-2,3-diene. A model may be helpfulSupply the missing reagent in the following reaction: (see attachment) A. Lindlar, H2, mCPBA B. O3 or KMnO4 C. fused KOH D. NH3 E. NaNH2Fill in the missing reagents below.
- reagents and reaction conditions draw second product that can also form from part bShow how HC≡CH, CH3CH2Br, and (CH3)2CHCH2CH2Br can be used to prepare CH3CH2C≡CCH2CH2CH(CH3)2. Show all reagents, and use curved arrows to show movement of electron pairs.a) Write out the 3-step arrow pushing mechanism showing how 1-pentene is hydrated to make 2-pentanol. b) Draw the other 2 alkenes(don’t forget cis/trans isomers!) that could also be hydrated to make 2-pentanol. Briefly explain why1-pentene is the best choice.
- 2-Methylpropane have more than one kind of hydrogen and will generate 2 different products with bromination in the presence of uv light. t or fExplain why a Büchner funnel is used to isolate the final crystallized product instead of stem funnel.Complete the following reaction: Pb+2 + SO4 -2 ---------------