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Interpretation:
‘change of energy’ should be identified.
Concept introduction:
From the Bohr postulates the radius of an orbit and its energy can be determined but to explain the atomic spectra the orbital concept have to introduce. The energy gap between the successive orbitals can be determined from the energy expression and the corresponding energy needed to excite an electron from a particular orbital to other orbital give rise the wave numbers which is associated with some particular spectrum. In the figure it is shown n = 1 to infinity.
The electron jumps from n=1 to n=2 is called the 1st excitation and n=2 to n=3 is 2nd excitation and like that. It is seen that as the number of n increases the energy gap between the successive orbitals decreases. The energy required to jump one electron from n=1 to n= infinity is called the ionisation energy of the atom.
Given:
In the
Where r = radius of the orbit, Z is the charge of the nucleus and
Bohr also concluded the energy level E of an electron in a given orbit is
To determine:
The difference of energy i.e.
The relation of the derived equation with the Balmer-Rydberg equation.
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Chapter 5 Solutions
Chemistry, Books a la Carte Edition and Modified Mastering Chemistry with Pearson eText & ValuePack Access Card (7th Edition)
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- Question 4 Determine the rate order and rate constant for sucrose hydrolysis. Time (hours) [C6H12O6] 0 0.501 0.500 0.451 1.00 0.404 1.50 0.363 3.00 0.267 First-order, k = 0.210 hour 1 First-order, k = 0.0912 hour 1 O Second-order, k = 0.590 M1 hour 1 O Zero-order, k = 0.0770 M/hour O Zero-order, k = 0.4896 M/hour O Second-order, k = 1.93 M-1-hour 1 10 ptsarrow_forwardDetermine the rate order and rate constant for sucrose hydrolysis. Time (hours) [C6H12O6] 0 0.501 0.500 0.451 1.00 0.404 1.50 0.363 3.00 0.267arrow_forwardDraw the products of the reaction shown below. Use wedge and dash bonds to indicate stereochemistry. Ignore inorganic byproducts. OSO4 (cat) (CH3)3COOH Select to Draw ઘarrow_forward
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- 2. Propose a mechanism for this reaction. ہلی سے ملی N H (excess)arrow_forwardSteps and explanationn please.arrow_forwardProblem 5-48 Assign R or S configurations to the chirality centers in ascorbic acid (vitamin C). OH H OH HO CH2OH Ascorbic acid O H Problem 5-49 Assign R or S stereochemistry to the chirality centers in the following Newman projections: H Cl H CH3 H3C. OH H3C (a) H H H3C (b) CH3 H Problem 5-52 Draw the meso form of each of the following molecules, and indicate the plane of symmetry in each: OH OH (a) CH3CHCH2CH2CHCH3 CH3 H3C. -OH (c) H3C CH3 (b) Problem 5-66 Assign R or S configurations to the chiral centers in cephalexin, trade-named Keflex, the most widely prescribed antibiotic in the United States. H2N H IHH S Cephalexin N. CH3 CO₂Harrow_forward
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