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- Identify the major organic product(s) of the following reaction. x A. B. 1) KOH D. ه (2 مسلسل موسلی yas2. How many different ß-hydroxyaldehydes and ß-hydroxyketones, including constitutional isomers and stereoisomers, are formed upon treatment of a mixture of acetone and benzaldehyde with base? a. b. 2 c. 3 d. 4What is the major organic product obtained from the following reaction? A. B. CI لله مللی حمله C. D. في
- Complete the following reactions by providing missing reagents or products: i.A. B. 2. Propose an efficient synthesis for each of the following transformations using any additional reagents(b) Draw a stepwise mechanism for the following transformation from A to B. This reaction is one of the key steps in a synthesis of lysergic acid diethyl amide (aka LSD). CI A CH ₂ AIC13 B CH₂ several steps away from lysergic acid diethyl amide (LSD)
- Give the missing reagentsComplete these reactions. (a) (b)Explain the reactivity and orientation effects observed in each heterocycle.a. Pyridine is less reactive than benzene in electrophilic aromatic substitution and yields 3-substituted products.b. Pyrrole is more reactive than benzene in electrophilic aromatic substitution and yields 2-substituted products.