1. Give the structure of the major product(s) in each of the following reactions. Give stereochemistry where appropriate. (a) (b) (c) Ph COOMe COOMe MCPBA (1 eq.) HCI (excess) Br₂ H₂O C B A
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- Represent the reaction equation of the alkene supplied to you with propanol, in acidic medium, indicating thestereochemistry of all the products formed.Provide the structure of the major organic product of the following reaction and? explain the stereochemistry which results in this product. 2-Pentanol reacting with 1.) PBr3, pyridine 2.) NaCNProvide one alkyl halide of your choice and discuss its structure, nomenclature (systematic and common), physical properties, method/s of preparation, and applications.
- Can you assist with predicting the organic product(s) of the last two reactions and provide stereochemistry, if applicable.Give the structure of the product and/or intermediates of the following reactions. Indicate, where appropriate, both regiochemistry and stereochemistry.(S)-2-Butanol, CH3CH2CHOHCH3, slowly racemizes on standing in dilute aqueous sulfuric acid. Explain, illustrating with a mechanism.
- Observe and identify what's the general reaction scheme and explain it.3. Obtain acetophenone and acetaldehyde by reaction of glycols with periodic acid. Justify your answer with the reaction mechanism.Wolff-Kishner reduction of compound W gave compound A. Treatment of A with m-chloroperbenzoic acid gave B which on reduction with LiAH4 gave C. Oxidation of compound C with chromic acid gave D (C9H14O). Suggest the structures for A, B, C, and D.