In each case below select the synthetic procedure that could be used to carry out the transformation shown **Title: Selecting Synthetic Procedures for Alkene Transformations****Description:**In each case below, select the synthetic procedure that could be used to carry out the transformation shown.**The procedures are:**1. **Epoxidation/Hydrolysis:** - Reactants: Alkene + meta-chloroperoxybenzoic acid - Follow-up: Hydrolysis with H₃O⁺2. **OsO₄ Oxidation:** - Reactants: Alkene + OsO₄ - Follow-up: Treatment with NaHSO₃**Transformation Diagrams:**1. **First Reaction:** - Starting Material: Contains a naphthalene ring with a single methyl group substituent. - Product: The same naphthalene ring with two hydroxyl groups (-OH) added to the top ring, one of which is attached to the methyl group.2. **Second Reaction:** - Starting Material: Cyclohexane ring with one methylene (-CH₂OH) group. - Product: Cyclohexane with an additional two hydroxyl groups, resulting in a triol.**Procedure Selection Options:**- Epoxidation/Hydrolysis- OsO₄ Oxidation- Both methods- Neither method**Interactivity:**Users can select one of the presented options via a dropdown menu for each transformation. Choices affect which synthetic method to use for the specific alkene transformation depicted.**Submission:**Users can submit their answers and have the option to retry the entire group of transformations if needed. There are 9 more group attempts remaining. **Image Transcription for Educational Website**In each case below, select the synthetic procedure that could be used to carry out the transformation shown.**The procedures are:**1. **Epoxidation/hydrolysis:** alkene + meta-chloroperoxybenzoic acid; then H₃O⁺2. **OsO₄ oxidation:** alkene + OsO₄; then NaHSO₃**Chemical Transformations:**1. **Transformation 1:** - **Starting Compound:** Cyclohexene with two methyl groups attached to the same carbon. - **End Compound:** Cyclohexane ring with two hydroxyl groups (OH) in a syn diol configuration on adjacent carbons.2. **Transformation 2:** - **Starting Compound:** A cyclopentane ring with an attached alkene chain (propene side chain). - **End Compound:** Cyclopentane ring with a 1,2-diol (two adjacent OH groups) added to the former alkene chain, forming an alcohol with a methyl group.**Dropdown Options for Each Transformation:**- Epoxidation/hydrolysis- OsO₄ oxidation- Both methods- Neither method**Interactive Features:**- "Submit Answer" button: To submit the selected procedure.- "Retry Entire Group" button: To attempt the exercises again.- Notification: "9 more group attempts remaining" indicates limited retries.This educational tool helps in understanding the application of two types of chemical reactions—epoxidation and OsO₄ oxidation—in synthesizing diols from alkenes.

Alkene is nucleophilic center which is attacked by an electrophile reagent and this reaction is known as electrophilic addition reaction at alkene.Osmium tetra oxide is oxidizing reagent, which react with alkene in cycloaddition manner in such a way that it goes for syn addition of alcohol in alkene. Therefore, the given reaction for syn addition of alcohol is given as: Therefore, the synthesis procedure for the reaction is OsO4Oxidation. Reaction of meta chloro peroxybenzoic acid in alkene produces a epoxied in alkene, then hydrolysis in presence of acid provides the trans addition of di-ol in the alkene. Therefore, given reaction with trans addition of alcohol is given by: Therefore, the synthesis procedure for the given reaction is epoxidation then hydrolysis.Reaction of meta chloro peroxybenzoic acid in alkene produces a epoxied in alkene, then hydrolysis in presence of acid provides the trans addition of di-ol in the alkene. Therefore, given reaction with trans addition of alcohol is given by: Therefore, the synthesis procedure for the given reaction is epoxidation then hydrolysis. When, there is no steriochemistry is provided then the di-ol production can be done by epoxidation then hydrolysis or by the oxidation with osmium tetra oxide. Therefore, the reaction is given as: Therefore, the synthesis procedure for the reaction is both.