Do question 2 do whichever letter is more convenient and explain. **Resonance and Reaction Practice***For extra practice with resonance, see the drawing resonance contributors tutorial on pages 382-389 of the textbook.*---1) **Resonance Structure Task:**- **Objective:** Draw an additional resonance structure for the following anion.- **Instructions:** Include curved arrows and indicate which resonance form is a greater contributor to the resonance hybrid.*Diagram: An alkoxide anion (ethoxide with a negative charge on the oxygen atom).*---2) **Reaction Practice:****Objective:** Give the major organic product of the following reactions.- **a)** Reaction of a styrene-like compound with \( \text{H}_3\text{O}^+ \).- **b)** Reaction of a cyclohexene with HBr at 40°C.- **c)** Reaction of a cyclohexene with HCl at -80°C.(Note: For each reaction, consider the conditions provided and apply your understanding of reaction mechanisms to predict the major product.)

An arrow always depicts from a region of high electron density to low electron density ; that is tail depicts region of high electron density and head depicts region of low electron density.A) This is an electrophilic addition reaction.It involves acid catalyzed addition of water across double bond to form more substituted alcohol.first step, electrophilic attack of proton takes place across double bond to form secondary carbocation.This undergoes 1,2-hydride shift to form more stable benzyl carbocation.In next step, water nucleophile attacks followed by proton transfer to form final product.C) This is an electrophilic addition reaction.In first step, electrophilic attack of proton takes place to form tertiary carbocation intermediate.chloride nucleophile attack to form final product.This is kinetically controlled product which depends on stability of carbocation. it forms at a faster rate and requires low activation energy.B) the initially formed carbocation can undergo rearrangement to form another carbocation which is more substituted.chloride nucleophile attacks this to form product.This is thermodynamically controlled product which depends on stability of final product, so requires high activation energy and is more stable.