### Organic Chemistry ReactionsBelow are the reaction schemes and reagents used for various organic transformations starting with a six-membered ring structure as the base compound.1. **Initial Reaction Scheme** - **Reactant:** Six-membered ring with one double bond (cyclohexene). - **Reagents:** 1. **Step 1:** O3 at -78°C (Ozonolysis). 2. **Step 2:** (CH3)2S (Dimethyl sulfide). - **Product:** Results in the cleavage of the double bond.2. **Oxidation Reaction Scheme** - **Reactant:** Six-membered ring with double bond. - **Reagents:** - KMnO4 in the presence of H2O and heat. - **Product:** This oxidizes the double bond.3. **Bromination Reaction Scheme** - **Reactant:** Six-membered ring with double bond. - **Reagent:** Br2 in a CCl4 solvent (Bromination). - **Product:** Forms a brominated compound.4. **Hydroboration-Oxidation Reaction Scheme** - **Reactant:** Six-membered ring with double bond. - **Reagents:** 1. Hg(OAc)2 in H2O. 2. NaBH4 (Sodium borohydride). - **Product:** Forms an alcohol through hydroboration-oxidation.### Diagram ExplanationThe diagram presents a schematic progression for different chemical reactions of a six-membered carbon ring (cyclohexene). Each reaction starts from the same base compound but proceeds with different reagents resulting in various products:1. **Ozonolysis**: Uses ozone and dimethyl sulfide to cleave the double bond.2. **Oxidation**: Potassium permanganate with water and heat to oxidize the ring.3. **Bromination**: Bromine in carbon tetrachloride to add bromine across the double bond.4. **Hydroboration-Oxidation**: **Title:** Predicting Major Products in Organic Reactions**Instructions:**Predict the major product for the following reactions, showing the correct stereochemistry and/or regiochemistry where applicable. Where requested, supply the reagents.**Reactions:**1. **Reaction 1:** - **Substrate:** Cyclohexene derivative (one alkene in the ring, with an ethyl group attached) - **Reagent:** \( \text{HBr} \) - **Reaction Arrow:** Indicates forward reaction 2. **Reaction 2:** - **Substrate:** Cyclohexene derivative (same as above) - **Reagents:** - **Primary Reagent:** \( \text{HBr} \) - **Secondary Reagent:** \( \text{ROOR} \) (organoperoxide) - **Reaction Arrow:** Indicates forward reaction 3. **Reaction 3:** - **Substrate:** Cyclohexene derivative (same as above) - **Reagents:** - **Primary Reagent:** \( \text{MCPBA} \) (meta-Chloroperoxybenzoic acid) - **Solvent:** \( \text{CH}_2\text{Cl}_2 \) (Dichloromethane) - **Reaction Arrow:** Indicates forward reaction 4. **Reaction 4:** - **Substrate:** Cyclohexene derivative (same as above) - **Reagents:** - **Primary Reagent:** \( \text{OsO}_4 \) (Osmium tetroxide) - **Secondary Reagent:** \( \text{H}_2\text{O}_2 \) (Hydrogen peroxide) - **Reaction Arrow:** Indicates forward reaction 5. **Reaction 5:** - **Substrate:** Cyclohexene derivative (same as above) - **Reagents:** - **Primary Reagent:** \( \text{CH}_2\text{I}_2 \) (Diiodomethane) - **Catalyst:** \( \text{Zn(Cu)} \) (Simmons-Smith reagent) - **Reaction Arrow:** Indicates forward reaction 6. **Reaction 6:** - **Substrate:** Cyclohexene derivative (same as above) - **Reagents

Alkene is an electron rich compound as well as an unsaturated compound which mainly gives…

Answered: Supply reajents (1) O3 (-78°c) (2)…

Science

Chemistry

Supply reajents (1) O3 (-78°c) (2) (CH3)a' KMaOy / Hz0 heat Brz (oulvent) (') Hg COAdla / Hzo (2) NABHY

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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Part A Find A,H for the combustion of ethanol (C2H60) to carbon dioxide and liquid water from the following data: the heat capacity of the bomb calorimeter is 34.65 kJ K1 and the combustion of 1.755 g of ethanol raises the temperature of the calorimeter from 294.21 K to 295.72 K ? A;H = 1373 kJ mol-1 Submit Previous Answers Request Answer X Incorrect; Try Again; 4 attempts remaining