Fill in the missing product, or reactant in the reactions below. If no reaction will happen, write “NOREACTION” in the product box. If multiple products can form, show the MAJOR product, taking care toillustrate stereochemistry as appropriate The image depicts a chemical reaction sequence. **Reaction Scheme:**- There is a box labeled "F" on the left side, which likely represents a starting material or an unspecified reactant.- The reactant is subjected to a two-step chemical transformation.**Steps:**1. **Reagent 1:** The first step involves a Grignard reagent, specifically an organomagnesium compound represented as `(cyclopropyl)MgCl`. 2. **Reagent 2:** This is followed by treatment with hydronium ion, `H3O+`, in the second step.**Product:**- The product on the right is a cyclic alcohol with a cyclohexane ring. Attached to the ring is a vinyl group (double-bonded carbon) and a hydroxyl group (OH) indicating an alcohol.- The structure also shows stereochemistry with a wedged bond suggesting the 3D orientation of the hydroxyl group. This transformation likely involves nucleophilic addition of the Grignard reagent to a carbonyl group in the starting material, followed by acidic workup to produce the final alcohol product. Grignard reagents are commonly used in organic synthesis to form carbon-carbon bonds.

Grignard reagents are the nucleophiles. Grignard reagent is organometallic compound that are carbon based nucleophiles react with the electrophilic carbon species. Reaction mechanism of Grignard reagent with the epoxides: Epoxides are the three membered cyclic ether that have a ring strain. The reaction with these epoxides is based on SN2 reaction where C-O bond break and form new C-C bond i.e the negatively charged oxygen atom in the epoxide produce alcohol product. Attack of nucleophile: The electron pair that is present in the C-Mg bond that act as nucleophile attack the least hindered carbon of the epoxides that act as electrophile. Protonation: The formed new C-C bond reacts with the proton from the acid and form O-H bond. There is inversion of configuration in this SN2 reaction. 1,2 epoxy cyclopentane reacts with the nucleophile 1-propene Magnesium chloride and form an intermediate product where C-C bond and also inversion of configuration takes place. This intermediate product i.e 2-(1-propene)cyclopentoxide ion undergoes protonation and form alcohol product 2-(1-propene)cyclopentanol.