Part 2 out of 2Devise a synthesis of the biaryl whereby the methyl substituted ring is used to form the organoborane needed for coupling. **How many routes are possible for Suzuki coupling of the aromatic rings?**2**Part 2 out of 2: Devise a synthesis of the biaryl whereby the methyl substituted ring is used to form the organoborane needed for coupling.**---### Synthesis of Methyl Substituted Ring- **Benzene** - Step [A,1] - Options: - HNO₃, H₂SO₄ - Pd(PPh₃)₄, NaOH - [1] NaNO₂, HCl; [2] H₂O - CH₃Cl, AlCl₃ - **Intermediate [A,1]** - Step [A,2] - Options: - Br₂, FeBr₃ - [1] Li; [2] B(OCH₃)₃ - H₂, Pd-C - [1] NaI; [2] CH₃I - **Intermediate [A,2]** - Step [A,3] - Options: - Pd(PPh₃)₄, NaOH - [1] Li; [2] B(OCH₃)₃ - Br₂, FeBr₃ - HNO₃, H₂SO₄ - **Methyl substituted aromatic ring**---### Synthesis of Methoxy Substituted Ring- **Benzene** - Step [B,1] - Options: - Br₂, FeBr₃ - CH₃Cl, AlCl₃ - H₂, Pd-C - [1] NaNO₂, HCl; [2] H₂O - **Intermediate [B,1]** - Step [B,2] - Options: - PCC - [1] NaI; [2] CH₃I - H₂, Pd-C - HNO₃, H₂SO₄ - **Intermediate [B,2]** - Step [B,3] - Options: - H₂, Pd-C - [1] NaNO₂, HCl; [2] H₂O - Pd(PPh

We have to synthesize the given biaryl compound. Concept: Suzuki coupling and aromatic reactions.The synthesis of the methyl-substituted benzene ring is shown belowThe required synthesis of the methoxy substituted aromatic ring is shown belowThe required coupling reaction is shown below