Which of the following alkenes will yield a ketone when reacted with ozone followed by reduction and hydrolysis with dim

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Which of the following alkenes will yield a ketone when reacted with ozone followed by reduction and hydrolysis with dim

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Which Of The Following Alkenes Will Yield A Ketone When Reacted With Ozone Followed By Reduction And Hydrolysis With Dim 1
Which Of The Following Alkenes Will Yield A Ketone When Reacted With Ozone Followed By Reduction And Hydrolysis With Dim 1 (104.58 KiB) Viewed 26 times
Which Of The Following Alkenes Will Yield A Ketone When Reacted With Ozone Followed By Reduction And Hydrolysis With Dim 2
Which Of The Following Alkenes Will Yield A Ketone When Reacted With Ozone Followed By Reduction And Hydrolysis With Dim 2 (114.45 KiB) Viewed 26 times
Which of the following alkenes will yield a ketone when reacted with ozone followed by reduction and hydrolysis with dimethyl sulfide? I. IV. a. II, III, and V Ob. I, III and V O c. III, IV, and V Od. I, II, and III II. V. III. Which alcohol is prepared from the reaction of 1-methylcyclohexene with borane followed by hydrogen peroxide in base? 1. 1-methylcyclohexanol 2. trans-2-methylcyclohexanol 3. cis-2-methylcyclohexanol 4. cis and trans 2-methylcyclohexanol What is a likely side product when trans-2-butene reacts with HCI in ethanol? 1. 2-chloro-3-ethoxybutane 2. dibutyl ether 3. sec-butyl ethyl ether 4. diisobutyl ether
Which of the following reagents give an electrophilic addition to alkenes? I. H2 and Pt II. HCI III. 10% H2SO4 IV. Br2 in CC14 V. 03 1. II, III and IV 2. I and II 3. II and III 4. I, IV and V Which of the following reagents add to an alkene in a Markovnikov orientation? I. HCI in water II. mercuric acetate in methanol III. diborane followed by hydrogen peroxide and base IV. aqueous sulfuric acid 1. I, II and IV 2. II and IV 3. I and II 4. I, III and IV Which of the following reactions with alkenes involve a free radical mechanism? I. hydrobromination with peroxides II. hydroboration III. photochemical bromination IV. expoxidation .......... 1. I and III 2. II and III 3. I and IV 4. III and IV
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