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A: The reaction given is aldol reaction.
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Q: What is the major enolate formed in each reaction ?
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Q: CH3NH2 H30* e) j) NaOEt Aldol Condensation
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Q: 24. Propose an efficient synthesis for each of the following transformation: Br > (a) OH (b)
A: The conversion is given as,
Q: Draw the structure of the major aldol product (prior to possible dehydration) of the following…
A: The reaction taking place is given as,
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A: Given reaction:
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A: The correct answer is given below
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Q: Upon treatment with Tollen's reagent, you would expect one of these compounds to be unreactive. OH…
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Q: OH OH Ni 25°C heat E2 H, H. aldol 1) LIAIH, 2) H,O*
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Q: CHO 1. HCN HO- 2. Hа/Pd но 3. H30* CH2OH +
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Q: 4. Propose a multistep synthesis for each of the following transformations: a) CN HO. b) Ph OTs
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Q: 2. (a) What is the major enolate formed in each reaction? Justify your prediction : LDA, THF -78 °C…
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Q: 1. Draw the main enolate that will be formed with the reaction conditions below? 25 °C CH3CH2OH +…
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A: Given:- We have to perform this conversion via a mechanism.
Q: Rank the following compounds toward increasing acidity as shown below CH3NO2 > CH3COCH3 > CH3COOCH3>…
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Q: the resulting aldol from the following? OH 2
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Q: 8. Provide a series of steps to accomplish the following transformation. CO₂Me Ph d
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Q: Which of the following will not undergo an aldol condensation reaction? Obutanal 2-methylbutanal…
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Q: Identify the enol form of each keto toutomer. A. HO. B. D1 C. B1 B. HO- D. D A1 HO. HO, C1
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Q: What product is obtained from the aldol condensation of cyclohexanone?
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identify the reagents that will accomplish the following eneatioselective transformation
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