Interpretation:
The wavelength (in meters) of light emitted when an electron in a hydrogen atom goes from
Concept Introduction:
The emission of radiation given by an energized hydrogen atom to the electron falling from a higher-energy orbit to a lower orbit give a quantum of energy in the form of light. Based on electrostatic interaction and law of motion, Bohr derived the following equation.
Where,
The electrons are excited thermally when the light is used by an object. As a result, an emission spectrum comes. Line spectra consist of light only at specific, discrete wavelengths. In emission, the electron returns to a lower energy state from
This transition results in the photon’s emission with frequency
When,
The speed, wavelength and frequency of a wave are interrelated by
Substitute the frequency formula and rearrange,
Therefore, this formula is used to find the wavelength of the given photon in the emission line process. For the absorption line process in which an electron is removed from the nucleus, the sign is changed as,
To calculate: The wavelength (in meters) of light emitted when an electron in a hydrogen atom goes from
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Chapter 3 Solutions
CHEMISTRY: ATOMS FIRST VOL 1 W/CONNECT
- Add curved arrows to the reactants in this reaction. A double-barbed curved arrow is used to represent the movement of a pair of electrons. Draw curved arrows. : 0: si H : OH :: H―0: Harrow_forwardConsider this step in a radical reaction: Br N O hv What type of step is this? Check all that apply. Draw the products of the step on the right-hand side of the drawing area below. If more than one set of products is possible, draw any set. Also, draw the mechanism arrows on the left-hand side of the drawing area to show how this happens. O primary Otermination O initialization O electrophilic O none of the above × ☑arrow_forwardNonearrow_forward
- Can I get a drawing of what is happening with the orbitals (particularly the p orbital) on the O in the OH group? Is the p orbital on the O involved in the ring resonance? Why or why not?arrow_forward1) How many monochlorination products-including stereochemistry- are there for the molecule below:arrow_forwardSelect an amino acid that has and N-H or O-H bond in its R-group (you have 8 to choose from!). Draw at least two water molecules interacting with the R-group of the amino acid.arrow_forward
- Is this aromatic?arrow_forwardCHEM2323 E Tt PS CH03 Draw and name all monobromo derivatives of pentane, C5H11Br. Problem 3-33 Name: Draw structures for the following: (a) 2-Methylheptane (d) 2,4,4-Trimethylheptane Problem 3-35 (b) 4-Ethyl-2,2-dimethylhexane (e) 3,3-Diethyl-2,5-dimethylnonane (c) 4-Ethyl-3,4-dimethyloctane 2 (f) 4-Isopropyl-3-methylheptane KNIE>arrow_forwardProblem 3-42 Consider 2-methylbutane (isopentane). Sighting along the C2-C3 bond: (a) Draw a Newman projection of the most stable conformation. (b) Draw a Newman projection of the least stable conformation. Problem 3-44 Construct a qualitative potential-energy diagram for rotation about the C-C bond of 1,2-dibromoethane. Which conformation would you expect to be most stable? Label the anti and gauche conformations of 1,2- dibromoethane. Problem 3-45 Which conformation of 1,2-dibromoethane (Problem 3-44) would you expect to have the largest dipole moment? The observed dipole moment of 1,2-dibromoethane is µ = 1.0 D. What does this tell you about the actual conformation of the molecule?arrow_forward
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