For the following reaction: a. Draw the missing starting material b. Show the complete stepwise mechanism to reaction the product shown. Hll +enantiomer 2. CH,OH
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A: a.
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Q: 1. i) Fill in the boxes with the missing reagent(s). ii) Label each reaction as an "oxidation" or…
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Q: 4. What is the product of the following reaction? EtONa For the reaction in problem 4, draw a…
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Q: Dehydration of 1,2,2-trimethylcyclohexanol with H2SO4 affords 1-tert-butylcyclopentene as a minor…
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Q: Draw a stepwise mechanism for the conversion of dihalide A and cyclohexane-1,4-diol to polyether B…
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A: Given incomplete reaction is : What is the starting material = ?
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- Explain why a Büchner funnel is used to isolate the final crystallized product instead of stem funnel.N-Chlorosuccinimide (NCS) serves as a source of Cl+ in electrophilic addition reactions to alkenes and alkynes. Keeping this in mind, draw a stepwise mechanism for the following addition to but-2-yne.Show the SN2 mechanism in the reaction between (S) 2-bromobutane and iodide ion. Label the product and draw a enery diagram for this reaction.
- Spiderweb chemistry . Reagents needed to get the major product and show stereochemistry.Why some substituents make a benzene ring react faster than benzeneitself (activators) ?What kind of reagent is KmnO4? Draw the possible reactions of this reagent with the specific compounds tested in the following reaction?
- Explain why Jone's oxidation of 4-methyl-2-pentanol is faster than that of 3,3-dimethyl-2-pentanol.Whats the reason for the girgnard reagent attack that carbon of starting point in this step? a. Bc it gives us desired product b. Due to the sterics c. Bc it is more electrophilic than the other carbon of the starting pointDevise a stepwise mechanism for the conversion of M to N. N has been converted in several steps to lysergic acid, a naturally occurring precursor of the hallucinogen LSD (Figure 16.4).
- Draw the major organic product for the reaction between 1,2-dimethylcycloheptene and a cold, dilute solution of KMnO4.a.What product(s) (excluding stereoisomers) are formed when Y is heated with Cl2? b.What product(s) (excluding stereoisomers) are formed when Y is heated with Br2? c.What steps are needed to convert Y to the alkene Z?Show the arrow pushing mechanism using the reagents (1) Pd/C, H2 (2) H2SO4