a) b) c) H2N. но. но. CO₂Me ОН ... IIIIS Me Me Me Ph 1) Оз; Ме2S 2) NaBH4 H2SO4, H2O PCC H2 HO. НО, CO₂Me Me Me OH OH Me Ph

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A:

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Q: A) Suggest two possible syntheses for the following target molecule (TM), starting with any aldehyde…

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Q: The -NH, group is listed in our textbook as the strongest o,p-directing activator in electrophilic…

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Q: 12) Using the conmmpounds in the box, propose a synthesis for compounds 40, 41 and 42. You can use…

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Q: Draw all possible resonance structures of acetanilide. Looking at your resonance structures,…

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Q: a. What reagent(s) are needed to synthesize the enamine below. Also, draw the resonance structure(s)…

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Q: 24. Predict the major product of the reaction below. Next, draw a complete curved arrow mechanism…

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Q: Provide the alkyl bromide and nucleophile/base needed to produce the following compound. If your…

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Q: НО ОН

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Q: 22. a. Label the reactive features, highlight the most reactive one, then highlight what it needs.…

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Q: Calculate [H*], [CIO,], and [OH¯]in an aqueous solution that is 0.165 M in HC1O,(aq) at 25 °C.

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A: A ketone can be reduced to alcohol by mild reducing agent such as NaBH4

Q: Draw a major resonance contributor of this enolate anion. Include all lone pairs in your structure.…

A:

Q: reasons 2. Analyse following C₂H5 C₂H5 C₂H Ph C₂H5 "COOH NH

A: Concept behind the reaction Synthesis for the above Target molecule the reaction that needed are…

Q: Step 2: Complete the resonance structure of the keto form, then add curved arrows.   Step 3:…

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Q: Explain why the nitrogen in an amide is not a good nucleophile. Use a picture to show why

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Q: Choose the correct statement(s) regarding Aryl halides participation in NAS reactions. The rate of…

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Q: BS21008 Organic Chemistry for the Life Sciences Assignment Week 7 Bearing in mind Huckel's rule,…

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Q: ester, amide, acid anhydride. Explain your logic. You should include : 1) the order in decreasing…

A: Nucleophilic acyl substitution: