Chapter 2: Q.2-2-35_C (page 59)
Question: Calculate the formal charges on the atoms shown in red.

Short Answer
Answer
The formal charge on C is 0.
The formal charge on N bonded with C is +1
The formal charge on N bonded with N is -1
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Chapter 2: Q.2-2-35_C (page 59)
Question: Calculate the formal charges on the atoms shown in red.

Answer
The formal charge on C is 0.
The formal charge on N bonded with C is +1
The formal charge on N bonded with N is -1
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The following molecular models are representations of (a) adenine and (b) cytosine, constituents of DNA (deoxyribonucleic acid). Indicate the positions of multiple bonds and lone pairs for both, and draw skeletal structures (gray 5 C, pink 5 O, blue 5 N, ivory 5 H).

Imidazole forms part of the structure of the amino acid histidine and can act as both an acid and a base.

Imidazole Histidine
(a)Look at the electrostatic potential map of imidazole, and identify the most
acidic hydrogen atom and the most basic nitrogen atom.
(b)Draw structures for the resonance forms of the products that result when
imidazole is protonated by an acid and deprotonated by a base.
Draw electron-dot structures for the following molecules, indicatingany unshared electron pairs. Which of the compounds are likely to actas Lewis acids and which as Lewis bases?
(a)(b) (c)
(d)HF (e)(f)
Question: Calculate formal charges for the non-hydrogen atoms in the following molecules:
(a)Diazomethane,H2C=N=N:
(b)Acetonitrile oxide, H3C-CN-O
(c) Methyl isocyanides,H3CNC:
We’ll see in the next chapter that organic molecules can be classified according to the functional groups they contain, where a functional group is a collection of atoms with a characteristic chemical reactivity. Use the electronegativity values given in Figure 2-2 on page 29 to predict the direction of polarization of the following functional groups.

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