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- predict the product of each of the following reactions. Mono-halogenated products only for any radical halogenation reactions.Explain why free-radical halogenation usually gives mixture of products.Heterocyclic compounds plays an important role in our daily life. They are mainly used in pharmaceutical and agrochemical products to name a few. 3. It is required to introduce a halogen group to a five membered ring, thiophene. Discuss the reaction mechanism involved in the reaction by selecting a suitable halogen group and analyze why a particular substituted product obtained after the reaction is predominant over the other possible product(s) with the help of reactions.
- Predict the major product(s) for each of the following electrocyclic reactions. Justify your answer with MO theory. Draw the frontier orbitals involved. hv hv HeatPlease explain the reaction mechanism above to show how product is formed. The product is the borate coplymer .( Please include ALL lone pairs with the structures and provide an explanation of what is happening)Give the reaction mechanism and explain in detail. Also perform the woodward Hoffman analysis to explain the selectivity and geometry of the product.
- Predict the major products of the following reaction. Be sure to use wedge and dash bonds to show the stereochemistry of the products when it's important, for example to distinguish between two different major products...Can you please predict the MAJOR product or provide the reagents/conditions for the following reactions? Please indicate racemic if it is and if there is no reaction, please specify that as well. ?piperidine undergoes the series of reactions shown here, 1,4-pentadiene is obtained as the product. When the four different methyl-substitutedpiperidines undergo the same series of reactions, each forms a different diene: 1,5-hexadiene; 1,4-pentadiene; 2-methyl-1,4-pentadiene; and3-methyl-1,4-pentadiene. Which methyl-substituted piperidine forms which diene?
- Give only typing answer with explanation and conclusion What are the correct reaction conditions for the following transformation?Determine an efficient reaction scheme required to complete each of the following reactions.Suggest a reason why wittig reactions usually give mixtures of cis and trans isomers. which of the cis or trans isomer is the. major product? explain.