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- 4. Draw the possible resonance structures for compounds C and D. Include lone pairs and indicate non-zero formal charges. Circle the minor resonance contributor for compound C. O :O: :O: C & DHydrocarbon A possesses a signicant dipole, even though it is composed of only C–C and C – H bonds. Explain why the dipole arises and use resonance structures to illustrate the direction of the dipole. Which ring is more electron rich?Draw out all resonance structures for each structure below. + NH₂
- Shown below is a heterocylic aromatic compound. How many more aromatic aromatic resonance forms exist? [HINT: Copy the structure, use one or more curved arrow and assess all possible structures.] H N H3CkomalDraw a resonance structure, complete with all formal charges and lone (unshared) electron pairs, that shows the resonance interaction of the carboxy with the para position in benzoic acid.

