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- Draw out all resonance structures for each structure below. + NH₂Draw the contributing resonance structures for the following. ЕНHydrocarbon A possesses a significant dipole, even though it iscomposed of only C—C and C—H bonds. Explain why the dipole arisesand use resonance structures to illustrate the direction of the dipole.Which ring is more electron rich?
- Question 18 Determine whether the following compounds are aromatic, anti-aromatic or neither. BH anti-aromatic aromatic neither6. Draw all significant resonance structures for the following compound, including curved arrows to indicate the movement of electrons. HC || CH-CH-C=CH HC.Bond-line Formula IUPAC Name m. n. он
- With reference to compound A below, label each compound as an identical molecule, an isomer, a resonance structure, or neither. Compound A CH2 identical molecule resonance structure neither isomer4. Circle the following pairs of structures that do not constitute resonance structures. For the proper resonance pairs, draw curved arrows to convert the first structure to the second. Draw in all lone pairs of electrons. H3C-CH3 „CH3 HgC-N' a) b) H2C=C=CH2 H3C-CECH FCH2 d) H3C' CH2 H H3CDraw all significant resonance structures for the following compound: O