Determine a reasonable synthetic scheme for a multi step synthesis using substitution, elimination, and Elrctrophile addition to non polar pi bonds. Explain. (Can you visually show me, im a visual learner) ?
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- Heterolytic cleavage of the CO bond to yield a carbocation.p. please don't provide handwrriten solution Write the mechanism of the reaction with proper arrow formalisim, do not combine into one stepWhen considering electrophilic 3 points aromatic substitution reactions, aldehydes are described as... Ortho/para directing and activating Meta directing and activating. Para directing and deactivating Meta directing and deactivating Ortho/para directing and deactivating O O
- Give a detailed explanation on the reaction of tje compound and its mechanism and why did it happen. (see attached picture)Give a clear handwritten mechanism and product for given below Sn2 reaction..a reaction shows all bonds ,lone pairs and arrows...?Alkyl diazonium salts decompose to form carbocations, which go on to form products of substitution, elimination, and (sometimes)rearrangement. Keeping this in mind, draw a stepwise mechanism thatforms all of the following products