(4) 2. Write the structure of the key intermediate and the product (with correct stereochemistry) for reaction of N-Bromosuccinimide (NBS) with cyclopentene in aqueous DMSO BromosuCcinir су NBS DMSO H,O Intermediate Product
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I got the answer but I just want to check if i got it right. Can you show the mechanism?
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- Arrange the structure on the image with regard to the reactivity towards hydrolysis. 1 being the least and 3 being the mostWhen the nitrogen-containing aromatic heterocyclic compounds 1 and 2 are treated with HCl, only 1 forms the hydrochloride salt, whereas compound 2 is unreactive. Provide an explanation for this observed reactivity.If you oxidatively degraded lignin and were able to separate the following aldehyde inreasonable yield and purity, which other compound(s) could you derive from it, usingredox chemistry?
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