Question

There may be a peak or peaks in your spectrum for which you are unable to...

There may be a peak or peaks in your spectrum for which you are unable to assign a transition in the Balmer series. What might such an unknown peak be due to?

Homework Answers

Answer #1

Ans :-

When we record any spectrum, there will be some unwanted peaks due to electric or electronic or surrounding disturbances. This is called noise. Balmer series is formed in visible light region during the electronic transition between two energy levels. So, if you observe a peak in visible region and it it's energy is not equal to the difference in any two energy levels of the atom for which the spectrum has been studied, then we can not assign the peak to balmer series of that atomic spectrum.

So,

Here such an unknown peak could be due to the surrounding light.

Know the answer?
Your Answer:

Post as a guest

Your Name:

What's your source?

Earn Coins

Coins can be redeemed for fabulous gifts.

Not the answer you're looking for?
Ask your own homework help question
Similar Questions
1. In the ferrocene spectrum, why is there only 1 peack(ignoring TMS and other non-relevant peaks?...
1. In the ferrocene spectrum, why is there only 1 peack(ignoring TMS and other non-relevant peaks? 2. In the acetyl ferrocene spectrum, how could your tell which peak(s) belong to the acetylated ring, and whcih peak(s) belong tothe non-acetylated ring? 3. IN the diacetylferrocene spectrum, how could you predict which peak correspons to the Hs adjacent to the acetyl group, and whcih peak corresponds tothe aromatic Hs futher away from the acetyl group? Please help!
In an 1H NMR spectrum using CDCl3, you observe a broad peak at 1.5ppm that is...
In an 1H NMR spectrum using CDCl3, you observe a broad peak at 1.5ppm that is not related to your product and integrates for 2.6 Hs relative to a methyl group. What could be responsible for this peak and what might this indicate about your sample?
A compound, C10H14, shows an IR peak at 745 cm-1. Its 1H NMR spectrum has peaks...
A compound, C10H14, shows an IR peak at 745 cm-1. Its 1H NMR spectrum has peaks at delta 7.18 (4 H, broad singlet), 2.70 (4 H, quartet, J=7 Hz), and 1.20 (6 H, triplet, J=7 Hz). Draw its structure in the window below. You do not have to consider stereochemistry. You do not have to explicitly draw H atoms. In cases where there is more than one answer, just draw one.
A few basic gas chromatography questions: In general, how would you determine which of several peaks...
A few basic gas chromatography questions: In general, how would you determine which of several peaks in a chromatogram obtained for a mouthwash sample might correspond to ethanol? (Is your suggested method 100% reliable?) How would you use that peak to determine how much ethanol is present in the mouthwash? In general, will an increase in operating temperature cause a given peak to have a longer or a shorter retention time? Why? In general, will a decrease in mobile phase...
so you anticipate any situations in which you may be unable to engage empathetically with an...
so you anticipate any situations in which you may be unable to engage empathetically with an individual Do you anticipate any situations in which you may be unable to engage empathetically with an individual in social work.
1.-Which of these choices best describes the interpretation of the following peak that may be recorded...
1.-Which of these choices best describes the interpretation of the following peak that may be recorded in a 1H NMR spectrum? 0.9? (3H, s). The quoted hydrogen atom is intended to be the one producing the peak that we are interpreting.                 A) O=C-C(C)2C’H’3                 B) O=C-CHC’H’3                 C) O=C-CH2C’H’3                 D) None of these interpretations describes this peak. 2.- Which of these choices best describes the interpretation of the following peak that may be recorded in a 1H NMR...
You are performing a separation experiment with gas chromatography and notice that your peaks have overlapping...
You are performing a separation experiment with gas chromatography and notice that your peaks have overlapping elution times. Provide three possible approaches you could take to improve the resolution of the peaks. Explain how these changes would provide a higher resolution using the resolution equation. Which of your listed approaches would be the most cost effective?
your compound is a liquid and you would like to obtain an IR spectrum. What options...
your compound is a liquid and you would like to obtain an IR spectrum. What options for running this sample do you have ? In each case indicate the reference you must remove so the spectrum is only that of your sample.
Each part of this question asks you about your knowledge of the hydrogen atom spectrum. Eatom...
Each part of this question asks you about your knowledge of the hydrogen atom spectrum. Eatom = -2.178 x10-18 J * (1/nf2 - 1/ni2) Part 1: Choose the electron transition that has the largest energy. A) n = 4 → n= 1 B) n = 3 → n= 2 C) n = 4 → n= 3 D) n = 4 → n= 2 E) n = 3 → n= 1 F) n = 2 → n= 1 Part 2: Choose...
A dc series motor is connected to a constant-toque load, which may be considered to require...
A dc series motor is connected to a constant-toque load, which may be considered to require a constant electromagnetic torque regardless of motor speed. Neglect the voltage drops due to the armature and series-field resistances, the armature reaction, and the effects of saturation. (a) By what percent is the motor speed changed wgen the line voltage is reduced from 230 V to 200 V? (b) Repeat (a), assuming a shunt motor. (c) State briefly what effects saturation might have on...