The cyclic voltammogram of the antibiotic chloramphenicol (abbreviated) is shown here. The first cathodic scan goes from 0 to -1.0 V. The first cathodic wave, , is from the reaction RNO2+4e-+4H+RNHOH+H2O. Peak B in the reverse anodic scan could be assigned to RNHOHRNO+2H++2e-. In the second cathodic scan from +0.9 to -0.4 V, the new peak C appears. Write a reaction for peak C and explain why peak C was not seen in the initial scan.


Cyclic voltammogram of 3.7 ×10-4 chloramphenicol in 0.1 M acetate buffer, pH 4.62. The voltage of the carbon paste working electrode was scanned at a rate of 350 mV/s. [Data from P. T. Kissinger and W. R. Heineman, “Cyclic Voltammetry,” J. Chem. Ed. 1983, 60, 702.]

Short Answer

Expert verified

The peak C is given in cyclic voltammogram

The reaction for peakC:RNO+2H++2e-RNHOH

Absence of RNO before initial scanning is the reason behind peak C was not seen before the initial scan.

Step by step solution

01

Introduction

Voltammetry is one type of electrochemical reactions which expresses the relationship between current and voltage. Voltammogram is the graph representing current vs voltage .

02

Determine the reaction between peak current and voltage for the given reaction.

Peak B: RNHOHRNO+2H++2e-

Peak C:RNO+2H++2e-RNHOH

During the first scan, Nitrate gets converted into hydrazine by reduction. In the anodic scan, it undergoes oxidation to give nitric oxide. Peak appears in the anodic scan. Peak C does not appear in the initial scan because nitric oxide forms only in anodic scan. Absence of RNO before initial scanning is the reason behind peak C was not seen before the initial scan

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Most popular questions from this chapter

What does a mediator do?

Coulometric titration of sulfite in wine. Sulfur dioxide is added to many foods as a preservative. In aqueous solution, the following species are in equilibrium:

Bisulfite reacts with aldehydes in food near neutral pH:


Sulfite is released from the adduct in 2MNaOH and can be analyzed by its reaction with I3- to give I-and sulfate. ExcessI3- must be present for quantitative reaction.

Here is a coulometric procedure for analysis of total sulfite in white wine. Total sulfite means all species in Reaction and the adduct in Reaction . We use white wine so that we can see the color of a starch-iodine end point.

1. Mix 9.00 mL of wine plus 0.8gNaOH and dilute to 10.00mL. The releases sulfite from its organic adducts.

2. Generate I3-at the working electrode (the anode) by passing a known current for a known time through the cell in Figure 17 - 10. The cell containsofacetate buffer () plus. In the cathode compartment, is reduced to H2+OH-. The frit retards diffusion of into the main compartment, where it would react with I3- to giveIO-.

3. Generate I3- at the anode with a current of for.

4. Inject 2.000mL of the wine/ solution into the cell, where the sulfite reacts with leaving excess.

5. Add of thiosulfate to consume by Reaction and leave excess thiosulfate.

6. Add starch indicator to the cell and generate freshI3- with a constant current of 10.0mA. A time of 131s was required to consume excess thiosulfate and reach the starch end point.

(a) In what pH range is each form of sulfurous acid predominant?

(b) Write balanced half-reactions for the anode and cathode.

(c) At pH 3.7, the dominant form of sulfurous acid isand the dominant form of sulfuric acid is HSO42-. Write balanced reactions between andand between I3-and HSO3-thiosulfate.

(d) Find the concentration of total sulfite in undiluted wine.

Write the chemical reactions that show that 1 mol of I2 is required for 1 mol of H2O in a Karl Fischer titration.

Explain how amperometric end-point detection in Figure17-9 operates.

In a coulometric Karl Fischer water analysis, 25.00 mL of pure "dry" methanol required 4.23 C to generate enough I2 to react with residual H2O in the methanol. A suspension of 0.8476 g of finely ground polymeric material in 25.00 mL of the same "dry" methanol required 63.16 C. Find the wt %H2O in the polymer.

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