(a)
Interpretation:
The magnitude of the force on the electron at each separation should be calculated.
Concept Introduction:
The formula which is used to calculate the force between proton and electron separated by distance is given by:
Where,
Z =
r is the distance between proton and electron.
(b)
Interpretation:
The change in potential energy between the proton and electron should be calculated.
Concept Introduction:
The energy which is possessed by an object or material due to its composition or position with respect to other objects or materialis said to be potential energy
The formula which is used to calculate the potential energy between electron and proton separated by distance is given by:
Where,
r is the distance between the proton and electron.
(c)
Interpretation:
The change in the speed of the electron should be calculated when the electron was initially stationary.
Concept Introduction:
The following formula is used for calculating the change in speed of the electron is:
Where, m = mass of electron (
r = radius of the electron (
h = Planck’s constant (
n = principal quantum number
The relation between radius and principal quantum number is:
Where,
Z = atomic number
n = principal quantum number
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Chapter 3 Solutions
Bundle: Principles of Modern Chemistry, Loose-leaf Version, 8th + LMS Integrated for OWLv2 with MindTap Reader, 4 terms (24 months) Printed Access Card
- For the SN2 reaction, draw the major organic product and select the correct (R) or (S) designation around the stereocenter carbon in the organic substrate and organic product. Include wedge-and-dash bonds and draw hydrogen on a stereocenter. Η 1 D EN Select Draw Templates More C H D N Erasearrow_forwardQ9: Explain why compound I is protonated on O while compound II is protonated on N. NH2 NH2 I IIarrow_forwardAN IR spectrum, a 13 CMR spectrum, and a 1 HMR spectrum were obtained for an unknown structure with a molecular formula of C9H10. Draw the structure of this compound.arrow_forward
- AN IR spectrum, a 13 CMR spectrum, and a 1 HMR spectrum were obtained for an unknown structure with a molecular formula of C9H10. Draw the structure of this compound.arrow_forward(a) What is the hybridization of the carbon in the methyl cation (CH3*) and in the methyl anion (CH3¯)? (b) What is the approximate H-C-H bond angle in the methyl cation and in the methyl anion?arrow_forwardQ8: Draw the resonance structures for the following molecule. Show the curved arrows (how you derive each resonance structure). Circle the major resonance contributor.arrow_forward
- Q4: Draw the Lewis structures for the cyanate ion (OCN) and the fulminate ion (CNO). Draw all possible resonance structures for each. Determine which form for each is the major resonance contributor.arrow_forwardIn the following molecule, indicate the hybridization and shape of the indicated atoms. CH3 N CH3 HÖ: H3C CI: ::arrow_forwardQ3: Draw the Lewis structures for nitromethane (CH3NO2) and methyl nitrite (CH3ONO). Draw at least two resonance forms for each. Determine which form for each is the major resonance contributor.arrow_forward
- Q1: Draw a valid Lewis structures for the following molecules. Include appropriate charges and lone pair electrons. If there is more than one Lewis structure available, draw the best structure. NH3 Sulfate Boron tetrahydride. C3H8 (linear isomer) OCN NO3 CH3CN SO2Cl2 CH3OH2*arrow_forwardQ2: Draw all applicable resonance forms for the acetate ion CH3COO. Clearly show all lone pairs, charges, and arrow formalism.arrow_forwardPlease correct answer and don't used hand raitingarrow_forward
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