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Question: The purine heterocycle occurs commonly in the structure of DNA.

a. How is each N atom hybridized?

b. In what type of orbital does each lone pair on a N atom reside?

c. How many πelectrons does purine contain?

d. Why is purine aromatic?

Short Answer

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Answer

a. The hybridization of each nitrogen in purine is sp2.

b. The unlabeled nitrogen atoms are sp2hybridized and have lone pairs in one of the sp2hybrid orbitals. The labeled nitrogen has its lone pair in a p orbital.

c. Purine contains 10πelectrons.

d. Purine is aromatic as it is cyclic, planar, conjugated, and has 4n+2π electrons.

Step by step solution

01

Purines

Purine is a compound comprising nitrogen as a heteroatom and falls under the category of heterocyclic compounds. These compounds form part of the DNA, and the different kinds of purine include adenine and guanine.

02

Aromatic compounds

Several properties of aromatic compounds are given below:

  • Each atom in the ring possesses a p orbital for the delocalization of electron density.
  • Aromatic compounds are not subjected to the addition reactions of alkenes
03

Purine heterocycle

a.

Purine heterocycle with labeled and unlabeled nitrogens

The nitrogen atom noted with an asterisk is surrounded by three groups and possesses a lone pair. This lone pair takes place in the delocalization of electrons. The other nitrogen atoms are surrounded by two groups and have one lone pair. Hence the hybridization of each nitrogen is sp2.

b. The three hydrogens that are not labeled with an asterisk aresp2 hybridized, possessing lone pair of electrons in one of the sp2hybrid orbitals. The nitrogen marked with an asterisk contains lone pair of electrons in a p orbital.

c. The purine molecule has 4π bonds and a lone pair of electrons. According to Huckel’s rule, the number of pi electrons is given by 4n+2π electrons, where n indicates a whole number. The value of 4n+2 can be calculated as:

4n+2=4×2+2=10π

d. For a compound to become aromatic, it must be cyclic, planar, completely conjugated, and contain 4n+2π electrons. Purine is cyclic, planar, completely conjugated, and includes 10πi.e.4×2+2π electrons. Hence, it is an aromatic molecule.

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Most popular questions from this chapter

Question: Stanozolol is an anabolic steroid that promotes muscle growth. Although stanozolol has been used by athletes and bodybuilders, many physical and psychological problems result from prolonged use and it is banned in competitive sports.

a. Explain why the nitrogen heterocycle—a pyrazole ring—is aromatic.

b. In what type of orbital is the lone pair on each N atom contained?

c. Draw all reasonable resonance structures for stanozolol.

d. Explain why the pKaof the N-H bond in the pyrazole ring is comparable to the pKa of O-H bond, making it considerably more acidic than amines such as CH3NH2( pKa= 40).

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Question: Would [16]-, [20]- or [22]-annulene be aromatic if each ring is planar?

Question: Use the inscribed polygon method to show the pattern of molecular orbitals in cyclooctatetraene.

a. Label the MOs as bonding, antibonding, or nonbonding.

b. Indicate the arrangement of electrons in these orbitals for cyclooctatetraene, and explain why cyclooctatetraene is not aromatic.

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d. How are the πelectrons in this dianion arranged in the molecular orbitals?

e. Classify the dianion of cyclooctatetraene as aromatic, antiaromatic, or not aromatic, and explain why this is so.

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