When the molecule below is treated with HCI, the product distribution shown is obtained. Use curved arrow formalism to draw a mechanism for this process. Account for the product distribution and draw resonance structures for relevant intermediates. HCI Cl &.& + 85% 15% CI
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- Please don't provide handwritten solution... Give the major product and mechanism for the following reaction:(a) Provide a detailed mechanism for the reaction below. Explain any selectivity issues that arise. Ms = ---S -Me OMS CI + PhMgBr .CIGive detailed mechanism of the reaction in clear handwritten! Use arrows to show mechanism.
- predict the major products of the following reactions. İf it possible, write all steroisomersA compound X is bitter in taste. It is a component of washing powder& reacts withdil. HCI to produce brisk effervescence dur to colourless, odourless gas Y wich turns lime water milky due to formation of Z. When excs of CO2is passed, ilkinessdisappears due to formation of P. Identify X, Y, And Z & P.Which of the following best describes a key step in the mechanism for the reaction below? HO, ... -CH3 -CH3 + en dihydroxylation H3C- H3C- OH (A) free-radical substitution at the carbonyl carbon B elimination reaction by abstraction of a beta-hydrogen nucleophilic attack by an alkene to form a cyclic (epoxide) intermediate electrophilic addition reaction to form a carbocation intermediate
- please provide the missing organic materials starting materials, reagents/reactions, conditions or organic products in the reaction below. kindly provide and show ther eaction mechanism as wellProvide the complete mechanism using curved arrow formalism for the reaction of p-isopropxlbenzoic acid undergoing nitration. Tell how many peaks in the 'H and 13C NMR spectrum that would be observed for the final product.Help me please