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A: pH = 8.90-6pOH =14 -8.90 = 5.10pOH =-log[OH-][OH-]= 10-5.10 = 7.9432 *10-6 M Mg(OH)2…
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- 32. Propose a mechanism for the following reaction: H30*6. Provide the missing products for the following reactions: CH,OH, H CH,MgBr Ph,P=CHCH PCC HO Na₂Cr₂O H₂O° CrO, H₂SO H₂OWhich reaction would produce the proposed product in a good yield? H NaBH, MeOH Н,О, Н,О OH НО ОН Н НО, Н,О 1. CH,MgBr 2. 1,0 HO OH X НО ОН х
- 4. Give the starting alkene and any other reagents needed to selectively make the following compounds (with no organic byproducts!): OH L Eto OH all OH Br Br BrWhat is the expected product of the reaction shown? H3C 1(CH3)2NH 2.H20 H3C. он N(CH3)2 OH H;C ZHN" H;C OH (H;C),N IV II CH3 OI O II OIV3- What products are obtained by the hydration of the following Alkyne: CH3CH₂CH₂C=CCH₂CH₂CH3 4- Write the complete mechanism of Li NH3 Reduction of an Alkyne. Show the directions of the electron flow with the proper arrow orientations. Name the final Product. DA ☎ 6 Z 76
- Use your general knowledge of alkene chemistry to suggest a mechanism for the following reaction.Propose a curved-arrow mechanism to show how ozone (O3) reacts with a carbon-carbon double bond to form a molozonide, the first intermediate in ozonolysis.Draw the structures of the organoboranes formed when borane reacts with each alkene below, including the regiochemistry and stereochemistry as appropriate. Propose a mechanism for each reaction.
