
General Chemistry: Principles and Modern Applications (11th Edition)
11th Edition
ISBN: 9780132931281
Author: Ralph H. Petrucci, F. Geoffrey Herring, Jeffry D. Madura, Carey Bissonnette
Publisher: PEARSON
expand_more
expand_more
format_list_bulleted
Question
Chapter 10, Problem 134SAE
Interpretation Introduction
Interpretation:
The species with triple bond from the given list of species needs to be determined.
Concept introduction:
A triple bond is a bond with two atoms involving six bonding electrons. The bond length of a triple bond is shorter than single or double bond. The strength of the bond is inversely proportional to bond length thus; triple bond is stronger than double bond which is then stronger than single bond.
Expert Solution & Answer

Want to see the full answer?
Check out a sample textbook solution
Students have asked these similar questions
Answe Answer A and B please
3. Refer to the data below to answer the following questions:
Isoelectric point
Amino Acid
Arginine
10.76
Glutamic Acid
3.22
Tryptophan
5.89
A. Define isoelectric point.
B. The most basic amino acid is
C. The most acidic amino acid is
sidizo zo
3. A gas mixture contains 50 mol% H2 and 50 mol% He.
1.00-L samples of this gas mixture are mixed with
variable volumes of O2 (at 0 °C and 1 atm). A spark is
introduced to allow the mixture to undergo complete
combustion. The final volume is measured at 0 °C and 1
atm. Which graph best depicts the final volume as a
function of the volume of added O2?
(A)
2.00
1.75
Final Volume, L
1.50
1.25
1.00
0.75
0.50
0.25
0.00
0.00
0.25
0.50
2.00
(B)
1.75
1.50
Final Volume, L
1.25
1.00
0.75
0.50-
0.25
0.00
0.75
1.00
0.00
0.25
Volume O₂ added, L
2
0.50
0.75
1.00
Volume O₂ added, L
2
2.00
2.00
(C)
(D)
1.75
1.75
1.50
1.50
Final Volume, L
1.25
1.00
0.75
0.50
Final Volume, L
1.25
1.00
0.75
0.50
0.25
0.25
0.00
0.00
0.00
0.25
0.50
0.75
1.00
0.00
0.25
Volume O₂ added, L
0.50
0.75
1.00
Volume O₂ added, L
2
Chapter 10 Solutions
General Chemistry: Principles and Modern Applications (11th Edition)
Ch. 10 - Write Lewis symbols for the following atoms. (a)...Ch. 10 - Write Lewis symbols for the following ions. (a)...Ch. 10 - Write plausible Lewis structures for the following...Ch. 10 - Each of the following molecules contains at least...Ch. 10 - By means of Lewis structures, represent bonding...Ch. 10 - Which of the following have Lewis structures that...Ch. 10 - Prob. 7ECh. 10 - Suggest reasons why the following do not exist as...Ch. 10 - Describe what is wrong with each of the following...Ch. 10 - Describe what is wrong with each of the following...
Ch. 10 - Prob. 11ECh. 10 - Indicate what is wrong with each of the following...Ch. 10 - Write Lewis structures for the following ionic...Ch. 10 - Under appropriate conditions, both hydrogen and...Ch. 10 - Derive the correct formulas for the following...Ch. 10 - Each of the following ionic compounds consists of...Ch. 10 - Assign formal charges to each of the atoms in the...Ch. 10 - Assign formal charges to each of the atoms in the...Ch. 10 - Both oxidation state and formal charge involve...Ch. 10 - Prob. 20ECh. 10 - Prob. 21ECh. 10 - Assign formal charges to the atoms in the...Ch. 10 - Prob. 23ECh. 10 - Show that the idea of minimizing the formal...Ch. 10 - Write acceptable Lewis structures for the...Ch. 10 - Two molecules that have the same formulas but...Ch. 10 - The following polyatomic anions involve covalent...Ch. 10 - Represent the following ionic compounds by Lewis...Ch. 10 - Write a plausible Lewis structure for...Ch. 10 - Prob. 30ECh. 10 - Write Lewis structures for the molecules...Ch. 10 - Write Lewis structures for the molecules...Ch. 10 - Write Lewis structures for the molecules...Ch. 10 - Write Lewis structures for the molecules...Ch. 10 - Identify the main group that the element X belongs...Ch. 10 - Prob. 36ECh. 10 - Use your knowledge of electronegativities, but do...Ch. 10 - Which of the blowing molecules would you expect to...Ch. 10 - What is the percent ionic character of each of the...Ch. 10 - Prob. 40ECh. 10 - Prob. 41ECh. 10 - Use a cross-base arrow () to represent the...Ch. 10 - Which electrostatic potential map corresponds to...Ch. 10 - Prob. 44ECh. 10 - Two electrostatic potential maps are shown, one...Ch. 10 - Prob. 46ECh. 10 - Prob. 47ECh. 10 - Which of the following species requires a...Ch. 10 - Dinitrogen oxide (nitrous oxide, or "laughing...Ch. 10 - The Lewis structure of nitric acid, HONO2, is a...Ch. 10 - Draw Lewis structures for the following species,...Ch. 10 - Draw Lewis structures for the following species,...Ch. 10 - Write plausible Lewis structures for the following...Ch. 10 - Write plausible Lewis structures for the following...Ch. 10 - Which of the following species would you expect to...Ch. 10 - Write a plausible Lewis structure for NO2 , and...Ch. 10 - In which of the following species is it necessary...Ch. 10 - Prob. 58ECh. 10 - Use VSEPR theory to predict the geometric shapes...Ch. 10 - Use VSEPR theory to predict the geometric shapes...Ch. 10 - Each of the following is either linear, angular...Ch. 10 - Predict the geometric shapes of (a) CO ; (b)...Ch. 10 - One of the following ions has a trigonal-planer...Ch. 10 - Two of the following have the same shape. Which...Ch. 10 - Prob. 65ECh. 10 - Sketch the probable geometric shape of molecule of...Ch. 10 - Use the VSEPR theory to predict the shapes of the...Ch. 10 - Use the VSEPR theory to predict the shape of (a)...Ch. 10 - The molecular shape of BF2 is planar (see Table...Ch. 10 - Explain why it is not necessary to find the Lewis...Ch. 10 - Comment on the similarities and differences in the...Ch. 10 - Comment on the similarities and differences in the...Ch. 10 - Draw a plausible Lewis structure for the following...Ch. 10 - Draw a plausible Lewis structure for the following...Ch. 10 - Sketch the propyne molecule, CH2CCH. Indicate the...Ch. 10 - Sketch the propene molecule, CH2CHCH2. Indicate...Ch. 10 - Lactic acid has the formula CH2CH(OH)COOH. Sketch...Ch. 10 - Levulinic acid has the formula CH2(CO)CH2CH2COOH....Ch. 10 - Prob. 79ECh. 10 - Prob. 80ECh. 10 - Predict the shapes of the following molecules, and...Ch. 10 - Which of the blowing molecules would you expect to...Ch. 10 - The molecule H2O2 has a resultant dipole moment of...Ch. 10 - Prob. 84ECh. 10 - Without referring to tables in the text, indicate...Ch. 10 - Estimate the lengths of the blowing bonds and...Ch. 10 - A relationship between bond lengths and...Ch. 10 - In which of the following molecules would you...Ch. 10 - Prob. 89ECh. 10 - Prob. 90ECh. 10 - A reaction involved in the formation of ozone the...Ch. 10 - Use data from Table 10.3, but without performing...Ch. 10 - Use data from Table 10.3 to estimate the enthalpy...Ch. 10 - One of the chemical reactions that occurs in the...Ch. 10 - Estimate the standard enthalpies of formation at...Ch. 10 - Prob. 96ECh. 10 - Use bond energies from Table 10.3 to estimate rH...Ch. 10 - Equations (1) end (2) can be combined to yield the...Ch. 10 - One reaction involved in the sequence of reactions...Ch. 10 - Prob. 100ECh. 10 - Given the bond-dissociation energies:...Ch. 10 - Prob. 102IAECh. 10 - Prob. 103IAECh. 10 - Prob. 104IAECh. 10 - Prob. 105IAECh. 10 - Draw Lewis structures for two different molecules...Ch. 10 - Sodium azide, NaN2 is the nitrogen gas-forming...Ch. 10 - Prob. 108IAECh. 10 - Prob. 109IAECh. 10 - A few years ago the synthesis of a salt containing...Ch. 10 - Prob. 111IAECh. 10 - In certain polar solvents, PCI, undergoes an...Ch. 10 - Prob. 113IAECh. 10 - Prob. 114IAECh. 10 - Use the VSEPR theory to predict a probable shape...Ch. 10 - The standard enthalpy of formation of...Ch. 10 - Prob. 117IAECh. 10 - Prob. 118IAECh. 10 - Prob. 119IAECh. 10 - R. S. Mulliken proposed that the electronegativity...Ch. 10 - When molten sulfur reacts with chlorine gas, a...Ch. 10 - Hydrogen azide, HN2 , can exist in two forms. One...Ch. 10 - Prob. 123IAECh. 10 - Prob. 124IAECh. 10 - Prob. 125IAECh. 10 - One of the allotropes of sulfur is a ring of eight...Ch. 10 - One of the allotropes of phosphorus consists of...Ch. 10 - In this problem, we examine the basis of three...Ch. 10 - Prob. 129FPCh. 10 - Prob. 130FPCh. 10 - Prob. 131SAECh. 10 - Briefly describe each of the following ideas: (a)...Ch. 10 - Explain the important distinctions between (a)...Ch. 10 - Prob. 134SAECh. 10 - The formal charges on the O atoms in the ion...Ch. 10 - Which molecule is nonlinear?...Ch. 10 - Which molecule is nonpolar?...Ch. 10 - The highest bond-dissociation energy is found in...Ch. 10 - The greatest bond length is found in...Ch. 10 - Draw plausible Lewis structures for the blowing...Ch. 10 - Predict the shapes of the following...Ch. 10 - Which of the following ionic compounds is composed...Ch. 10 - Which of the following molecules does not obey the...Ch. 10 - Which of the following molecules has no polar...Ch. 10 - The electron-group geometry of H2O is (a)...Ch. 10 - For each of the following compounds, give the...Ch. 10 - Use bond enthalpies from Table 10.3 to determine...Ch. 10 - Prob. 148SAECh. 10 - Prob. 149SAECh. 10 - What is the VSEPR theory? On what physical basis...Ch. 10 - Prob. 151SAECh. 10 - Prob. 152SAECh. 10 - Prob. 153SAECh. 10 - Prob. 154SAE
Knowledge Booster
Similar questions
- Leucine is an essential amino acid with the systematic name 2-amino-3-methylpentanoic acid. It has pai 2.36 and pKa2 = 9.60. H2N-C(R)H-COOH and R is -CH2-CH(CH3)2 A. Draw the condensed structure for leucine, and label all chirality centers with an asterisk. B. How many possible stereoisomers of leucine are there? C. Draw a Fischer projection of L-leucine and label the chirality center(s) as R or S. D. What is the p/ of leucine? E. Draw the structure of the predominant form of leucine at 10.00. F. Draw the structure of the predominant form of leucine at pH = 1.50. G. Leucine is described as an essential amino acid. What does this mean? H. Show the alkyl halide you would use to prepare leucine by the amidomalonate method. =arrow_forwarda) Write out 6 completely different reactions of acetophenone (reagent, product). b) Write out 3 preparations of 1-methylcyclohexanol, using a different starting material for each one. You may use preps where you just change the functional group, and/or preps where you construct the carbon chain. c) Write out 3 preparations of 2-ethoxybenzoic acid, a different starting material for each one. You may use preps where you just change the functional group, and/or preps where you construct the carbon chain.arrow_forward12. CH3 OH OH H&C CH3 H₂C N OH H₂C CH3 H&C CH3 H₂C' CH3 H.C CH3OH H.C CH2CH3OH CH3CEN Which one of these 17 compounds is represented by this IR and this 'H NMR spectrum? IR Spectrum 3000 4000 3000 NMR Spectrum 2000 £500 RAVENUMBER 2000 1500 9 8 6 5 10 HP-00-290 ppm m 1000 500 1000 4 °arrow_forward
- Draw the structure of (E,6R) 6-methoxy-4-hepten-2-one. Give the IUPAC name of this compound, including stereochemistry. Draw the most stable chair conformation of (cis) 1,3-isobutylcyclohexane. H HC=CCH₂ CH2CH3 EN(CH3)2 -CN(CH3)2arrow_forward10. Write out the mechanism (intermediate/transition state) for this reaction; indicate stereochemistry in product. H3C CH₂OH CH3 SN1 Harrow_forwardWrite "most" under the member of each trio which is most stable. Write "least under the member of each trio which is least stable. b) Draw a Fischer projection of a pair of enantiomers with three chiral carbons. Which of these two would you expect to be more soluble in water? Why? 1-butanol 1-heptanol Which of these two would you expect to have the higher boiling point? Why? hexyl methyl ether 1-heptanolarrow_forward
- Write "most" under the most acidic compound. Write "least" under the least acidic compound. OH NO₂ OCH3 Br 9. Compound X, C50H84F2, reacts with excess H2/Pd to give a C50H88F2 compound. How many rings are in X? How many double bonds are in X? Show your work.arrow_forward4. State whether these two are: a) the same molecule b) c) d) different compounds that are not isomers constitutional isomers diastereomers e) enantiomers CH3 CH₁₂ H OH HO H H OH HO H CH, CH₂ 5. a) How many stereocenters does this compound have? b) How many stereoisomers are possible for this compound? CH₂ OH CHCHarrow_forwardCalculating the pH at equivalence of a titration A chemist titrates 210.0 mL of a 0.1003 M hydrobromic acid (HBr) solution with 0.7550M KOH solution at 25 °C. Calculate the pH at equivalence. Round your answer to 2 decimal places. Note for advanced students: you may assume the total volume of the solution equals the initial volume plus the volume of KOH solution added. pH = ] ☑ o0o 18 Ararrow_forward
- Do you do chemistry assignmentsarrow_forwardUsing the conditions of spontaneity to deduce the signs of AH and AS Use the observations about each chemical reaction in the table below to decide the sign (positive or negative) of the reaction enthalpy AH and reaction entropy AS. Note: if you have not been given enough information to decide a sign, select the "unknown" option. reaction observations conclusions A This reaction is always spontaneous, but proceeds slower at temperatures above 120. °C. ΔΗ is (pick one) AS is (pick one) ΔΗ is (pick one) B This reaction is spontaneous except above 117. °C. AS is (pick one) ΔΗ is (pick one) This reaction is slower below 20. °C than C above. AS is |(pick one) ? 18 Ar 1arrow_forwardCalculating the pH at equivalence of a titration Try Again Your answer is incorrect. 0/5 a A chemist titrates 70.0 mL of a 0.7089 M hydrocyanic acid (HCN) solution with 0.4574M KOH solution at 25 °C. Calculate the pH at equivalence. The pK of hydrocyanic acid is 9.21. Round your answer to 2 decimal places. Note for advanced students: you may assume the total volume of the solution equals the initial volume plus the volume of KOH solution added. pH = 11.43] G 00. 18 Ar B•arrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
- Chemistry: The Molecular ScienceChemistryISBN:9781285199047Author:John W. Moore, Conrad L. StanitskiPublisher:Cengage LearningChemistry & Chemical ReactivityChemistryISBN:9781337399074Author:John C. Kotz, Paul M. Treichel, John Townsend, David TreichelPublisher:Cengage LearningChemistry: Principles and PracticeChemistryISBN:9780534420123Author:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward MercerPublisher:Cengage Learning
- General Chemistry - Standalone book (MindTap Cour...ChemistryISBN:9781305580343Author:Steven D. Gammon, Ebbing, Darrell Ebbing, Steven D., Darrell; Gammon, Darrell Ebbing; Steven D. Gammon, Darrell D.; Gammon, Ebbing; Steven D. Gammon; DarrellPublisher:Cengage Learning

Chemistry: The Molecular Science
Chemistry
ISBN:9781285199047
Author:John W. Moore, Conrad L. Stanitski
Publisher:Cengage Learning

Chemistry & Chemical Reactivity
Chemistry
ISBN:9781337399074
Author:John C. Kotz, Paul M. Treichel, John Townsend, David Treichel
Publisher:Cengage Learning

Chemistry: Principles and Practice
Chemistry
ISBN:9780534420123
Author:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward Mercer
Publisher:Cengage Learning

General Chemistry - Standalone book (MindTap Cour...
Chemistry
ISBN:9781305580343
Author:Steven D. Gammon, Ebbing, Darrell Ebbing, Steven D., Darrell; Gammon, Darrell Ebbing; Steven D. Gammon, Darrell D.; Gammon, Ebbing; Steven D. Gammon; Darrell
Publisher:Cengage Learning