Question: Provide the following information about L-dopa.

a. Label all sp3hybridized C atoms.

b. Label all H atoms that bear a partial positive chargelocalid="1648291738174" (δ+).

c. Draw another resonance structure.

Short Answer

Expert verified

Answer

a.

b.

c.

Step by step solution

01

Step-by-Step Solution Step 1: Determination of sp3 hybridization

When one s (valence) and three p (valence) orbitals hybridize, they form a hybrid orbital called sp3.

02

 Step 2: Formation of the dipole on the atoms

A dipole is created when there is the formation of δ+andδ-charges on the atoms involved in the bond.

In the dipole, role="math" localid="1648290916861" δ+is assigned to the less electronegative atom, while δ-is assigned to the more electronegative atom.

03

Formation of resonance structure

The movement of pi electrons generates resonance structures. So, if the structure contains two alternate pi bonds, it can form a resonance structure by changing the pi electron’s place.

04

Information on L-dopa

a. Carbon has four valence electrons of which two are in the 2s orbital and the other two are in the 2p orbital. It hybridizes by transferring one electron from 2s to 2p, and hence enables sp3hybridization.

Carbon can form a maximum of 4 single bonds through this hybridization. Therefore, L-dopa contains only twosp3hybridized carbon atoms as they form four single bonds.

sp3hybridized carbon atoms

b. The partial positive chargeδ+generates upon hydrogen when it bonds with a more electronegative atom (O, N).

The highly electronegative atom attracts the shared pair of electrons towards itself and makes hydrogen partially electron deficient.

Therefore, the partial positive chargeδ+on hydrogen is shown adjacent to the most electronegative atoms, that is, nitrogen and oxygen which is shown below:

Representation of charges

c. The resonance structure of L-dopa is formed by the movement of pi electrons in the benzene ring and the acid group, as shown below:

Resonance structure

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Most popular questions from this chapter

Question: The principles of this chapter can be applied to organic molecules of any size. Answer the following questions about amoxicillin, an antibiotic from the penicillin family:

a. Predict the hybridization and geometry around each highlighted atom.

b. Label five polar bonds using the symbols δ+andδ- .

c. How many π bonds does amoxicillin have? Label them.

d. Find a C- H bond containing a carbon atom having a hybrid orbital with 33% s character.

Question: Answer the following questions about compound A:

  1. Label the shortest single bond.
  2. Label the longest single bond.
  3. Considering all the bonds, label the shortest bond.
  4. Label the weakest bond.
  5. Label the strongest bond.
  6. Explain why bond [1] and bond [2] are different in length, even though they are both single bonds.

Question: Convert each condensed formula to a Lewis structure

a.CH3(CH2)4CH(CH3)2b.(CH3)3CCH(OH)CH2CH3c.(CH3)2CHCHOd.(OHCH2)2CH(CH2)3C(CH3)2CH2CH3

Question: While the most common isotope of nitrogen has a mass number of 14 (nitrogen-14), a radioactive isotope of nitrogen has a mass number of 13 (nitrogen-13). Nitrogen-13 is used in PET (positron emission tomography) scans by physicians to monitor brain activity and diagnose dementia. For each isotope, give the following information: (a) the number of protons; (b) the number of neutrons; (c) the number of electrons in the neutral atom; (d) the group number; and (e) the number of valence electrons.

Question: Follow the curved arrows to draw a second resonance structure for each species.

a.

b.

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