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Draw a reasonable mechanism for the given reaction
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- Please give the main substitution product for each of the following reactions, and indicate the dominant mechanism: (a) 1-bromopropane + NaOCH3 → (b) 3-bromo-3-methylpentane + NaOC2H5 →9. Plan syntheses of the following compounds. You may use the given starting material and any compound containing three or fewer carbons. (a) OH (b) Br Br- (c) ✓ -OTS (d) OHProvide reagents
- (a) (b) НО (c) Draw the products: (d) HO OH SOH OH H CCH2OH H₂SO4 'OH H₂SO4 H2SO4 OH H2SO41. At what position and on what ring would you expect the following substances to undergo electrophilic substitution? (b) CH3 Br lel CH3 2. Rank the compounds in each group according to their reactivity toward electrophilic substitution. (a) Chlorobenzene, o-dichlorobenzene, benzene (b) p-Bromonitrobenzene, nitrobenzene, phenol (c) Fluorobenzene, benzaldehyde, 0-xylene (d) Benzonitrile, p-methylbenzonitrile, p-methoxybenzonitrileAt what position, and on what ring, would you expect the following substances to undergo electrophilic substitution? (a) oa CH3 (c) (b) H N. ota (d) Br CI "sa "or" CH3
- Predict the major product of the following reaction. (CH3)3C-OOH LOH TI[OCH(CH3)214 (-)-DET Dom -OH 11 OH Io ||| Ø OH IVDraww all possible organic products and kinds of reactions (SN1, SN2, E1, E2)Determine whether each of the following syntheses requires a reaction that alters the carbon skeleton. (a) (b) OH (c) (d) OCH,CH3 CH3 (e) OH (f) H,CO он H;CO. (g) H3CO, (h) H3CO. NO2 NO2