Principles of Modern Chemistry
8th Edition
ISBN: 9781305079113
Author: David W. Oxtoby, H. Pat Gillis, Laurie J. Butler
Publisher: Cengage Learning
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Chapter 5, Problem 23P
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Chapter 5 Solutions
Principles of Modern Chemistry
Ch. 5 - Which of the following combinations of quantum...Ch. 5 - Which of the following combinations of quantum...Ch. 5 - Label the orbitals described by each of the...Ch. 5 - Label the orbitals described by each of the...Ch. 5 - Estimate the probability of finding an electron...Ch. 5 - Using Table 5.2, write down the mathematical...Ch. 5 - How many radial nodes and how many angular nodes...Ch. 5 - How many radial nodes and how many angular nodes...Ch. 5 - Use the mathematical expression for the 2pz wave...Ch. 5 - (a) Use the radial wave function for the 3p...
Ch. 5 - Calculate the average distance of the electron...Ch. 5 - The helium ion He+ is a one-electron system whose...Ch. 5 - Spectroscopic studies show that Li can have...Ch. 5 - Spectroscopic studies of Li also show that...Ch. 5 - Spectroscopic studies show that Na can have...Ch. 5 - Using data from Problems 13 and 15, calculate the...Ch. 5 - Give the ground-state electron configurations of...Ch. 5 - Give the ground-state electron configurations of...Ch. 5 - Prob. 19PCh. 5 - Write ground-state electron configurations for the...Ch. 5 - Identify the atom or ion corresponding to each of...Ch. 5 - Identify the atom or ion corresponding to each of...Ch. 5 - Predict the atomic number of the (as yet...Ch. 5 - (a) Predict the atomic number of the (as yet...Ch. 5 - Suppose that the spin quantum number did not...Ch. 5 - Suppose that the spin quantum number had three...Ch. 5 - Photoelectron spectra of mercury (Hg) atoms...Ch. 5 - Quantum mechanics predicts that the energy of the...Ch. 5 - Prob. 29PCh. 5 - Photoelectron spectroscopy studies of silicon...Ch. 5 - Photoelectron spectroscopy studies have determined...Ch. 5 - Prob. 32PCh. 5 - For each of the following pairs of atoms or ions,...Ch. 5 - For each of the following pairs of atoms or ions,...Ch. 5 - Predict the larger ion in each of the following...Ch. 5 - Prob. 36PCh. 5 - The first ionization energy of helium is...Ch. 5 - The energy needed to remove one electron from a...Ch. 5 - Without consulting any tables, arrange the...Ch. 5 - Both the electron affinity and the ionization...Ch. 5 - The cesium atom has the lowest ionization energy,...Ch. 5 - Until recently, it was thought that Ca was...Ch. 5 - In the hydrogen atom, the transition from the 2p...Ch. 5 - The energy needed to ionize an atom of element X...Ch. 5 - Suppose an atom in an excited state can return to...Ch. 5 - For the Li atom, the energy difference between the...Ch. 5 - How does the 3dxy orbital of an electron in O7+...Ch. 5 - The wave function of an electron in the lowest...Ch. 5 - An atom of sodium has the electron configuration...Ch. 5 - (a) The nitrogen atom has one electron in each of...Ch. 5 - Chromium(IV) oxide is used in making magnetic...Ch. 5 - Prob. 52APCh. 5 - Arrange the following seven atoms or ions in order...Ch. 5 - Which is higher, the third ionization energy of...Ch. 5 - The outermost electron in an alkali-metal atom is...Ch. 5 - In two-photon ionization spectroscopy, the...Ch. 5 - For the H atom, the transition from the 2p state...Ch. 5 - (a) Give the complete electron configuration...Ch. 5 - What experimental evidence does the periodic table...
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- 5. What is the product for the following reaction for each step and draw the mechanism H 1. NaNH2 2, EtBrarrow_forwardmical lation or mula trations, AAAAAAAAAAAAA Experiment #8 Electrical conductivity & Electrolytes Conductivity of solutions FLINN Scientific conductivity meter scale - RED LED Scale 0 Green LED OFF OFF 1 Dim OFF 2 medium OFF Bright Dim 4 Very Bright Medium 3 LED Conductivity Low or None' Low Medium High very high SE = Strong Electrolyte, FE = Fair Electrolyte WE Weak Electrolyte, NE= Noni Electrolyte 9 0.1 M NaOH. 10. 0.1M NH3 11. D.1M HCT 12. 0.1 M HC2H3D2 13 0 m H2SO4 Prediction observed conductivity ? Very bright red, dim green (4) ? Saturated Bright red, dim green 3 Cacal) Bright red, dim green 3 Prediction Bright red, No green ? observed Bright red,dim green ? Conductivity Just red? I Can you help me understand how I'm supposed to find the predictions of the following solutions? I know this is an Ionic compound and that the more ions in a solution means it is able to carry a charge, right? AAAAAA The light are not matching up with the scale So I'm confused about what I should be…arrow_forwardLabel these peaks in H- NMR and C- NMRarrow_forward
- Complete the following table. The only density needed is already given. Show your calculations in a neat and easy-to-follow manner in the space below the table. All units should be included and significant figures should be given close attention. Be sure to notice that the amount of material should be in millimoles rather than moles, and the theoretical mass of the product should in milligrams rather than grams. LOCH 3 + H2SO4 HNO 3 O=C-OCH 3 NO2 x H₂O F.W. 4.0 mL 1.3 M amount 0.50 mL in H2SO4 mg Theoretical Theoretical mmoles density 1.09arrow_forwardKumada Coupling: 1. m-Diisobutylbenzene below could hypothetically be synthesized by Friedel-Crafts reaction. Write out the reaction with a mechanism and give two reasons why you would NOT get the desired product. Draw the reaction (NOT a mechanism) for a Kumada coupling to produce the molecule above from m-dichlorobenzene. Calculate the theoretical yield for the reaction in question 2 using 1.5 g of p-dichlorobenzene and 3.0 mL isobutyl bromide. What signals appeared/disappeared/shifted that indicate that you have your intended product and not starting material? What other impurities are present in your product and how do you know?arrow_forwardWintergreen from Aspirin: 1. In isolating the salicylic acid, why is it important to press out as much of the water as possible? 2. Write the mechanism of the esterification reaction you did. 3. What characteristic absorption band changes would you expect in the IR spectrum on going from aspirin to salicyclic acid and then to methyl salicylate as you did in the experiment today? Give approximate wavenumbers associated with each functional group change. What signals appeared/disappeared/shifted that indicate that you have your intended product and not starting material? What other impurities are present in your product and how do you know?arrow_forward
- Synthesis of ZybanⓇ: 1. Write a mechanism for the bromination of m-chloropropiophenone. Br₂ CH2Cl2 Cl Br 2. Give the expected m/z (to a round number) for the molecular ion from the product above (including isotopic peaks). 3. What signals appeared/disappeared/shifted that indicate that you have your intended product and not starting material? What other impurities are present in your product and how do you know?arrow_forwardSynthesis of Ibuprofen-Part 2: 1. Some pain relievers including ibuprofen (MotrinⓇ) and naproxen (Aleve®) are "α-arylpropanoic acids." Look up the structure of naproxen (AleveⓇ), another a-arylpropionic acid. Using the same reactions that we used for making ibuprofen, show how to make naproxen from the compound below. Show all intermediates and reagents in your synthesis. Show how you would prepare ibuprofen starting from p-isobutylbenzene rather than p-isobutylacetophenenone. What reaction steps would need to change/add? 3. What signals appeared/disappeared/shifted that indicate that you have your intended product and not starting material? What other impurities are present in your product and how do you know?arrow_forwardAcid Catalyzed Aromatization of Carvone: 1. Starting with the ketone, below, draw a mechanism for the reaction to give the phenol as shown. H2SO4 HO- H₂O 2. Why do we use CDCl instead of CHCl, for acquiring our NMR spectra? 3. Why does it not matter which enantiomer of carvone is used for this reaction? What signals appeared/disappeared/shifted that indicate that you have your intended product and not starting material? What other impurities are present in your product and how do you know?arrow_forward
- Assign this H NMRarrow_forwardPlease complete these blanks need that asaparrow_forwardNitration of Methyl Benzoate: 1. Predict the major product for the reaction below AND provide a mechanism. Include ALL resonance structures for the intermediate. C(CH3)3 NO₂* ? 2. Assuming the stoichiometry is 1:1 for the reaction above, what volume of concentrated nitric acid would be required to mononitrate 0.50 grams of the compound above? What product(s) might you expect if you nitrated phenol instead of methyl benzoate? Explain your reasoning. What signals appeared/disappeared/shifted that indicate that you have your intended product and not starting material? What other impurities are present in your product and how do you know?arrow_forward
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