Predict the products please ### Organic Chemistry Reaction Pathways#### Reaction 1:- **Starting Material:** A benzene ring attached to a propyl chloride group.- **Reagents:** 1. Aluminum chloride (AlCl₃) 2. Water (H₂O)This reaction represents a Friedel-Crafts alkylation where the aluminum chloride acts as a catalyst to facilitate the formation of a carbocation, leading to the alkylation of the benzene ring.#### Reaction 2:- **Starting Material:** Cyclohexyl bromide.- **Reagents:** 1. Triphenylphosphine (PPh₃) 2. Butyllithium (BuLi) 3. CyclopentanoneThis sequence suggests a Wittig reaction pathway. The phosphonium salt formation with PPh₃ and BuLi allows for the generation of an ylide, which then reacts with the cyclopentanone to form an alkene.#### Reaction 3:- **Starting Material:** 1,2-cyclohexanediol- **Reagents:** - Excess pyridinium chlorochromate (PCC)This reaction describes an oxidation, where the diol is oxidized by PCC to form a diketone or an aldehyde, depending on the specifics of the reaction conditions and structure.These reactions showcase common transformations in organic synthesis, demonstrating mechanisms such as electrophilic aromatic substitution, ylide formation, and selective oxidation.

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Answered: .CI 1) AICI, 2) H,0 1) PPh, 2) BuLi Br…

Science

Chemistry

.CI 1) AICI, 2) H,0 1) PPh, 2) BuLi Br 3) OH excess PCC HO.

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

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