What is the mechanism for this reaction to produce Product 1? The product 1 is favored over product 2. Using orbital argument, explain why. Ziur N Product 1 scess N Product 2
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- Chemistry Use the table to identify which mechanism is favored by each factor and the overall factor that is favored. Also, what is the expected product?Heterolysis of the C–Z bond can generate a carbocation or a carbanion. Explain How ?Below is the equation for a nucleophilic substitution reaction and some experimental data. CH3CH2Br + CH3COO- ⇌ CH3CH2CO2CH3 + Br- ΔH=-75 kJ/mol Rate = k [CH3CH2Br][CH3COO-] Which reaction energy profile would be the best representative of the data provided?
- Draw an energy diagram for the SN2 reaction on the previous page. Your reaction coordinate diagram should: Include structures of starting materials, products, and transition states at correct relative energies. Indicate the activation energy of the rate determining step and whether the reaction is endothermic or exothermic. What makes this reaction endothermic or exothermic?Predict the structure of the rearranged carbocation. A) I B) II C) III D) IVBelow is the equation for a nucleophilic substitution reaction and some experimental data. CH3CH2Br + CH3COO- ⇌ CH3CH2CO2CH3 + Br- Rate = k [CH3CH2Br][CH3COO-] Which mechanism would best fit the data?
- Explain the possible mechanism (Sn1/Sn2/E1/E2) given the reaction. Show the transfer of electrons/groups, and name the product.1. which one is the starting material 2. what is the product/reaction 3. is it sn1 or sn2? (what is the reaction rate equation and mechanism?)1. Which among these would be the most stable carbocation?a. Allylicb. Vinylicc. Primaryd. Secondary2. What is the primary reason for the stability of tertiary carbocations?a. Free rotationb. Resonancec. Hyperconjugation
- Draw an energy diagram (potential energy versus reaction coordinate) for a typical SN1 reaction. Write the reaction using actual structures and propose the mechanism for a typical SN1 reaction of your choice.Draw the mechanism of the hydroboration reaction for 1-octene. Why are carbocation rearrangements not observed in this reaction?Explain the Carbocation Rearrangements ?