Chemistry: Principles and Practice
3rd Edition
ISBN: 9780534420123
Author: Daniel L. Reger, Scott R. Goode, David W. Ball, Edward Mercer
Publisher: Cengage Learning
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Chapter 10, Problem 10.27QE
(a)
Interpretation Introduction
Interpretation:
The bonded-atom lone-pair arrangement and the molecular shape of
(b)
Interpretation Introduction
Interpretation:
The bonded-atom lone-pair arrangement and the molecular shape of
(c)
Interpretation Introduction
Interpretation:
The bonded-atom lone-pair arrangement and the molecular shape of
(d)
Interpretation Introduction
Interpretation:
The bonded-atom lone-pair arrangement and the molecular shape of
(e)
Interpretation Introduction
Interpretation:
The bonded-atom lone-pair arrangement and the molecular shape of
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Cyanogen (CN)2 is known as pseodohalogen because it has some properties like halogens. It is composed of two CN’s joined together.(i) Draw the Lewis structure for all the possible combination for (CN)2.(ii) Calculate the formal charge and determine which one of the structures that you have drawn is most stable.(iii) For the stable structure, determine the geometry around the two central atoms.(iv) For the stable structure, draw the dipole arrows for the bonds.(v) Base on the stable structure, determine the polarity of molecule and state your reason.
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Chemical species are said to be isoelectronic if they have the same Lewis structure (regardless of charge). Consider these ions and write a Lewis structure for a neutral molecule that is isoelectronic with them. (a) CN–, (b) NH4+ (c) CO3 2–
Chapter 10 Solutions
Chemistry: Principles and Practice
Ch. 10 - Prob. 10.1QECh. 10 - Prob. 10.2QECh. 10 - Prob. 10.3QECh. 10 - Prob. 10.4QECh. 10 - Prob. 10.5QECh. 10 - Prob. 10.6QECh. 10 - Prob. 10.7QECh. 10 - Prob. 10.8QECh. 10 - Prob. 10.9QECh. 10 - Prob. 10.10QE
Ch. 10 - Which atomic orbitals overlap to form the bonds in...Ch. 10 - Prob. 10.12QECh. 10 - Identify the hybrid orbitals used by boron in BCl3...Ch. 10 - Identify the hybrid orbitals used by antimony in...Ch. 10 - Prob. 10.15QECh. 10 - Prob. 10.16QECh. 10 - Prob. 10.17QECh. 10 - Prob. 10.18QECh. 10 - Prob. 10.19QECh. 10 - Prob. 10.20QECh. 10 - Compare and contrast the molecular orbital and...Ch. 10 - Describe the bonding in molecular orbital terms...Ch. 10 - Prob. 10.23QECh. 10 - Prob. 10.24QECh. 10 - Prob. 10.25QECh. 10 - Prob. 10.26QECh. 10 - Prob. 10.27QECh. 10 - Prob. 10.28QECh. 10 - Prob. 10.29QECh. 10 - Prob. 10.30QECh. 10 - Prob. 10.31QECh. 10 - Prob. 10.32QECh. 10 - Prob. 10.33QECh. 10 - Prob. 10.34QECh. 10 - Prob. 10.35QECh. 10 - Prob. 10.36QECh. 10 - Prob. 10.37QECh. 10 - Prob. 10.38QECh. 10 - Prob. 10.39QECh. 10 - Use the VSEPR model to predict the bond angles...Ch. 10 - Prob. 10.41QECh. 10 - Prob. 10.42QECh. 10 - For each of the following molecules, complete the...Ch. 10 - Prob. 10.44QECh. 10 - Prob. 10.45QECh. 10 - Prob. 10.46QECh. 10 - Indicate which molecules are polar and which are...Ch. 10 - Prob. 10.48QECh. 10 - Indicate which of the following molecules are...Ch. 10 - Prob. 10.50QECh. 10 - Prob. 10.51QECh. 10 - Prob. 10.52QECh. 10 - Prob. 10.53QECh. 10 - Prob. 10.54QECh. 10 - Prob. 10.55QECh. 10 - Prob. 10.56QECh. 10 - Prob. 10.57QECh. 10 - Prob. 10.58QECh. 10 - Prob. 10.59QECh. 10 - Prob. 10.60QECh. 10 - Prob. 10.61QECh. 10 - Prob. 10.62QECh. 10 - Prob. 10.63QECh. 10 - Prob. 10.64QECh. 10 - Prob. 10.65QECh. 10 - Prob. 10.66QECh. 10 - Prob. 10.67QECh. 10 - Prob. 10.68QECh. 10 - Prob. 10.69QECh. 10 - Prob. 10.70QECh. 10 - Prob. 10.71QECh. 10 - Prob. 10.72QECh. 10 - Identify the orbitals on each of the atoms that...Ch. 10 - Prob. 10.74QECh. 10 - Prob. 10.75QECh. 10 - How many sigma bonds and how many pi bonds are...Ch. 10 - Give the hybridization of each central atom in the...Ch. 10 - Prob. 10.78QECh. 10 - Prob. 10.79QECh. 10 - Prob. 10.80QECh. 10 - Prob. 10.81QECh. 10 - Predict the hybridization at each central atom in...Ch. 10 - Prob. 10.83QECh. 10 - Tetrafluoroethylene, C2F4, is used to produce...Ch. 10 - Prob. 10.85QECh. 10 - Prob. 10.86QECh. 10 - Prob. 10.87QECh. 10 - Prob. 10.88QECh. 10 - Prob. 10.89QECh. 10 - Prob. 10.90QECh. 10 - Prob. 10.91QECh. 10 - Prob. 10.92QECh. 10 - Prob. 10.93QECh. 10 - Prob. 10.94QECh. 10 - Prob. 10.95QECh. 10 - Prob. 10.96QECh. 10 - Prob. 10.97QECh. 10 - Prob. 10.98QECh. 10 - The molecular orbital diagram of NO shown in...Ch. 10 - The molecular orbital diagram of NO shown in...Ch. 10 - The molecular orbital diagram of NO shown in...Ch. 10 - Prob. 10.102QECh. 10 - Prob. 10.103QECh. 10 - Prob. 10.104QECh. 10 - Prob. 10.105QECh. 10 - Following are the structures of three isomers of...Ch. 10 - The ions ClF2 and ClF2+ have both been observed....Ch. 10 - Aspirin, or acetylsalicylic acid, has the formula...Ch. 10 - Aspartame is a compound that is 200 times sweeter...Ch. 10 - Prob. 10.110QECh. 10 - Prob. 10.111QECh. 10 - Calcium cyanamide, CaNCN, is used both to kill...Ch. 10 - Histidine is an essential amino acid that the body...Ch. 10 - Formamide, HC(O)NH2, is prepared at high pressures...Ch. 10 - Prob. 10.115QECh. 10 - Prob. 10.116QECh. 10 - Prob. 10.117QECh. 10 - Prob. 10.118QECh. 10 - Prob. 10.119QECh. 10 - Prob. 10.120QECh. 10 - Prob. 10.121QECh. 10 - Prob. 10.122QECh. 10 - Prob. 10.123QECh. 10 - Prob. 10.124QECh. 10 - Two compounds have the formula S2F2. Disulfur...Ch. 10 - Prob. 10.126QECh. 10 - Prob. 10.127QE
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Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.Similar questions
- Consider the collection of nonmetallic elements O, P, Te,I, and B. (a) Which two would form the most polar singlebond? (b) Which two would form the longest single bond?(c) Which two would be likely to form a compound of formulaXY2? (d) Which combinations of elements would likelyyield a compound of empirical formula X2Y3?arrow_forwardCalculate the formal charge of each element in the following compounds and ions:(a) F2CO(b) NO–(c) BF4−(d) SnCl3−(e) H2CCH2(f) ClF3(g) SeF6(h) PO43−arrow_forwardWhich of these statements about resonance is true?(a) When you draw resonance structures, it is permissibleto alter the way atoms are connected.(b) The nitrate ion has one long N¬O bond and two shortN¬O bonds.(c) “Resonance” refers to the idea that molecules areresonating rapidly between different bonding patterns.(d) The cyanide ion has only one dominant resonancestructure.(e) All of the above are true.arrow_forward
- Which of the following molecules or ions contain polar bonds?(a) O3(b) S8(c) O22−(d) NO3−(e) CO2(f) H2S(g) BH4−arrow_forward(a) Describe the molecule xenon trioxide, XeO3, using four possible Lewis structures, one each with zero, one, two, or three Xe—O double bonds. (b) Do any of these resonance structures satisfy the octet rule for every atom in the molecule? (c) Do any of the four Lewis structures have multiple resonance structures? If so, how many resonance structures do you find? (d) Which of the Lewis structures in (a) yields the most favorable formal charges for the molecule?arrow_forward1. Draw the Lewis structures for each of the following ions or molecules. For each, give (i) the molecular shape, (ii) the electron pair geometry at the central atom, and (iii) the hybridization of the central atom. (a) POF3 (b) XeO₂F3+ (c) BrCl₂ (d) N3 (the central atom is N; two other N's are bonded to it) (e) PF3arrow_forward
- Identify the electron pair geometry and the molecular structure of each of the following molecules or ions:(a) IF6+(b) CF4(c) BF3(d) SiF5−(e) BeCl2arrow_forwardThe hypochlorite ion, ClO-, is the active ingredient inbleach. The perchlorate ion, ClO4-, is a main componentof rocket propellants. Draw Lewis structures for both ions. (a) What is the formal charge of Cl in the hypochlorite ion?(b) What is the formal charge of Cl in the perchlorate ion, assumingthe Cl—O bonds are all single bonds? (c) What is theoxidation number of Cl in the hypochlorite ion? (d) Whatis the oxidation number of Cl in the perchlorate ion, assumingthe Cl—O bonds are all single bonds? (e) In a redox reaction,which ion would you expect to be more easily reduced?arrow_forwardiv. Assign formal charges to the atoms in the following structures and decide which the more important contributor to the resonance hybrid is. (a) (b) H H C=N=N c-N=N H H v. What factor accounts for each of the following differences in bond length? (a) I, has a longer bond than Br,. (b) C-N bonds are shorter than C-C bonds. (c) H-C bonds are shorter than the C-O bond. (d) The C-O bond in formaldehyde, H,C=0, is longer than the bond in carbon monoxide, C=0.arrow_forward
- 19. :O: || :0-N- O: Which of the following statements, if true, would support the claim that the NO3 ion, represented above, has three resonance structures? (A) The NO3 ion is not a polar species. (B) The oxygen-to-nitrogen-to-oxygen bond angles are 90°. (C) One of the bonds in NO3 is longer than the other two. (D) One of the bonds in NO3¯ is shorter than the other two.arrow_forward(a) Describe the molecule xenon trioxide, XeO3, usingfour possible Lewis structures, one each with zero, one,two, or three Xe¬O double bonds. (b) Do any of theseresonance structures satisfy the octet rule for every atomin the molecule? (c) Do any of the four Lewis structureshave multiple resonance structures? If so, how many resonancestructures do you find? (d) Which of the Lewisstructures in part (a) yields the most favorable formalcharges for the molecule?arrow_forwardWhich compound has two or more resonance structures?(a) NO2- (b) CO2 (c) NH4+ (d) CCl4arrow_forward
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