Draw the product formed when the compound shown below undergoes a reaction with HBr in CH₂Cl₂. Interactive 3D display mode Draw the molecule on the canvas by choosing buttons from the Tools (for bonds), Atoms, and Advanced Template toolbars. The single bond is active by default. 0 0 ¹ ² CH3 (2 H2D EXP. CONT? Marvin JS Chomron IU ZOS-
Types of Chemical Bonds
The attractive force which has the ability of holding various constituent elements like atoms, ions, molecules, etc. together in different chemical species is termed as a chemical bond. Chemical compounds are dependent on the strength of chemical bonds between its constituents. Stronger the chemical bond, more will be the stability in the chemical compounds. Hence, it can be said that bonding defines the stability of chemical compounds.
Polarizability In Organic Chemistry
Polarizability refers to the ability of an atom/molecule to distort the electron cloud of neighboring species towards itself and the process of distortion of electron cloud is known as polarization.
Coordinate Covalent Bonds
A coordinate covalent bond is also known as a dative bond, which is a type of covalent bond. It is formed between two atoms, where the two electrons required to form the bond come from the same atom resulting in a semi-polar bond. The study of coordinate covalent bond or dative bond is important to know about the special type of bonding that leads to different properties. Since covalent compounds are non-polar whereas coordinate bonds results always in polar compounds due to charge separation.

### Task:
Draw the molecule on the canvas by choosing buttons from the Tools (for bonds), Atoms, and Advanced Template toolbars. The single bond is active by default.
#### Instructions:
1. Open the Marvin JS ChemAxon drawing canvas.
2. Utilize the toolbar to select the appropriate bonds and atoms.
- Tools: For drawing bonds.
- Atoms: For selecting atom types (carbon, hydrogen, etc.).
- Advanced Templates: For complex structures and ring systems.
3. Sketch the resulting compound after the reaction with HBr in CH₂Cl₂ is complete.
#### Example Toolbar:

### Expected Outcome:
After the addition reaction with HBr, the double bond of the cyclohexene will react with HBr, leading to the formation of a bromo-substituted cyclohexane. This addition reaction follows Markovnikov's rule where the hydrogen atom attaches to the carbon with more hydrogen atoms and the bromine attaches to the carbon with fewer hydrogen atoms.
Write out the molecular structure of the product achieving this addition.
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This exercise helps in understanding addition reactions in organic chemistry and using drawing tools to visualize complex molecular structures.](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Fcdfb37fd-3e7e-4c5b-b9de-8b4cda26a712%2F87d07c69-58ca-4d73-862e-2cfa1b7c6e19%2F7l83lr_processed.png&w=3840&q=75)
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