For 4-chlorophenol, For the carbon that would be the most likely location for the addition of OH radical, illustrate, with reactions and/or a chemical scheme a plausible mechanism that would lead to the production of the first stable hydroxylated product (i.e., just one OH radical addition). Show all steps, including reagents and side products (if any).
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- Indane can undergo free-radical chlorination at any of the alkyl positions onthe aliphatic ring. Once the products have been separated, what instrumental technique would be most helpful for determining the structures of all the dichlorinated products?can someone help me with this? Make a comparison table between the reaction mechanism SN1 and SN2, take into account thereaction order, nature of the substrates, solvents used, nature of the nucleophile, stereochemistry,kinetics, and other characteristics that you consider relevant.Label the reactive features of the following reactants, select the most reactive feature, thenwrite and highlight what it needs. Also, state if a carbocation, carbon radical, or carbanion willstart to develop, and/or if aromatic character will be lost as a result of a reaction between thesemolecules. cyclohexanone + 2 equivalents of methanol with acid
- Show the complete arrow pushing mechanism for this reaction and explain the originof the stereochemistry observed in the product.can i get help drawing out actual structures including the nucleophilic addition of Cy2NH to parafomaldehyde and its hemiaminal intermidiate and the condensation step when it is displaced by terminal alkyne forming allene, also what is dioxane getting rid of as the solvent, thanksthanks. Give the full mechanism for the reaction below that leads to the formation of the major monochlorinated product. Include the formation of the electrophile and all of the resonance stabilized arenium ion intermediates.
- For SN1 Explain the order in which 2o (secondary) alkyl halides reacted (fastest to slowest) and explain why. 2o (secondary) compounds listed are: (see picture) 2-chlorobutane 2-bromobutane bromobenzene bromocyclopentane bromocyclohexane Base your explanations on the following considerations: the nature of leaving group, the effect of structure, steric hindrance and any other feature. Be sure to explain which alkyl halides did not react and whyWrite suitable detailed mechanisms to account for the formation of the products in the following reactions, with arrows and proper stochiometry. Show all intermediates and any by products that are formed in these reactions.For SN2 Explain if 3o ( tertiary) alkyl halides reacted (fastest or slowest) explain why. Be sure to explain if alkyl halides did not react or did react and why. 3o (tertiary) compounds listed are: 2-chloro-2-methylpropane (see picture) Base your explanations on the following considerations: the nature of leaving group, the effect of structure, steric hindrance and any other feature.
- Provide reasonable mechanisms for the following reaction.Find the products for these two reactions. Make sure to include relevant hydrogens, deuteriums and stereohemistry.Step 2 of the iodination of benzene shows water acting as a base and removing a proton from the sigma complex. We did notconsider the possibility of water acting as a nucleophile and attacking the carbocation, as in an electrophilic addition to an alkene.Draw the reaction that would occur if water reacted as a nucleophile and added to the carbocation. Explain why this type ofaddition is rarely observed.