In radical reactions, there are sometimes non-halogenated side products formed from other termination steps. Choose the possible side product of the reaction shown below? || I A Y Br2 hv == B C III IV D IV
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- didentify the Allowry reactions, as substitution, elimination, or addition DrawWelection arrows to show how the in each reactors Circle and identify any reactive bands break & form intermediates of carbon. Ħ Br Br → AH-Br →→ → XB²What are the major products of this reaction? What is the reaction mechanism?Which chlorination product is formed via the lowest energy transition state in the rate-determining step? + CI-CI de .CI O All radical chlorinations require the same activation energies.
- Show the three step mechanism to form the major product only for the radical bromination shown below. label the initiation, propagation, and termination steps. draw the FULL electron pushing mechanism with ALL intermediates, lone pairs, and formal charges clearly labelled. Show ALL electron pushing arrows and label the nucleophile and electrophile where appropriate for non-radical mechanisms.I would like to understand how to mechanism of this reactions occurPlastic photochromic sunglasses are based on the following reversible rearrangement of a dye inside the lenses that occurs when the lenses are exposed to sunlight. The original dye absorbs UV light but not visible light and is thus colorless, while the rearrangement product absorbs visible light and is thus darkened. (a) Show the mechanism of the rearrangement. (b) Why does the rearrangement product absorb at a longer wavelength (visible light) than the original dye (UV)?
- Give detailed mechanism Solution with explanation needed. don't give Ai generated solutionBr tBuO H3C H3C CH2 H2 Alkyl halides undergo nucleophilic substitution and elimination reactions. When the kinetics of the reaction are measured, if the rate of the reaction is found alkyl halide the reaction is second order. The substitution reaction is thus termed SN2, and the elimination reaction is be dependent upon the concentration of the nucleophile as well as the termed E2. These reactions are bimolecular and take place in a single step. In the SN2 reaction, the nucleophile attacks the a-carbon from the backside and displaces the leaving group with an inversion of configuration occurring at the carbon. In the E2 elimination reaction, strong base removes an acidic hydrogen from the B-carbon and an alkene is formed as the leaving group is expelled from the a-carbon. This elimination follows Zaitsev's rule whereby the more substituted alkene is generally formed. In E2 elimination, both the B-hydrogen and the leaving group must be oriented anti to each other. The same reaction…Give detailed Solution with explanation needed
- Q15 Which of the given species or reaction steps, involved in a Grignard reaction, is not correct? Here, the species can be a reactant, intermediate, transition state, product, or byproduct. aj MgBr b) H₂0 Br :05 H *MgBr H HIn the reaction given below, what type of reaction is used?Consider the reaction coordinate diagram shown below. d)Is the overall reaction endothermic or exothermic? Briefly explain. e)Which step is the rate-determining step? Briefly explain.