draw arrows and products **Title: Mechanism of Bond-Breaking and Bond-Making in Organic Reactions****Instruction:**Be sure to account for all bond-breaking and bond-making steps.**Description:**This diagram illustrates a multi-step organic reaction mechanism involving sodium amide (NaNH₂) and alkyl bromide compounds. The process is outlined as follows:1. **Initial Reactants:** - The reaction begins with NaNH₂ interacting with an unspecified molecule containing hydrogen (H).2. **Step 1:** - **Reactants Diagram (Left):** A molecule with hydrogen atoms is illustrated. The instruction reads "Select to Add Arrows," indicating a visualization of the reaction mechanism. - **Conversion 1:** NaNH₂ is introduced, leading to bond-breaking and bond-making activities.3. **Step 2:** - **Middle Reaction Diagram (Center):** Following the introduction of NaNH₂, a new compound is formed with additional bromine presence (CH₃Br). - **Action 2:** Similarly, "Select to Add Arrows" prompts learners to visualize relevant mechanistic changes.4. **Step 3:** - **Reactants Diagram (Right):** The involvement of CH₃CH₂Br in the next step results in a molecule with a different arrangement. - **Conversion 2:** NaNH₂ once again participates, breaking and forming bonds to reach the final structure.**Educational Insight:**This mechanism underscores the significance of understanding each step in a reaction process, ensuring thorough comprehension of the movement of electrons and bonds during chemical transformations. It's crucial to select and depict proper arrows to convey the continuity and changes during the reaction. The image depicts a chemical reaction diagram focused on the process of ozonolysis. ### Description:#### Reaction Setup:- **Reactant**: The top section contains a line-angle chemical structure representing an organic compound with a carbon-carbon triple bond.- **Reagents**: 1. **O₃** (ozone) 2. **HOAc** (acetic acid)#### Reaction Process:An arrow points downwards, indicating the progression of the reaction with the reagents applied sequentially.#### Product Formation:Below the arrow are two dashed rectangles labeled "Select to Draw," indicating that the viewer would input or visualize the chemical structures of the compounds formed as a result of the ozonolysis reaction. The reaction is expected to yield carboxylic acids or aldehydes, depending on the specific carbon-chain structure being ozonolysed and on the reagents used.This diagram illustrates the ozonolysis process in organic chemistry, involving the cleavage of carbon-carbon multiple bonds using ozone, specifically in the presence of acetic acid.

Organic Reactions are given. We have to draw arrows and find out the products in the reactions.Sodium amide is a base and will abstract the acidic proton of alkyne. The alkyne ion formed will act as a nucleophile and attack on the electrophilic carbon atom of alkyl bromide.Ozonolysis of alkyne gives two carboxylic acid as product.