Chemistry & Chemical Reactivity
10th Edition
ISBN: 9781337399074
Author: John C. Kotz, Paul M. Treichel, John Townsend, David Treichel
Publisher: Cengage Learning
expand_more
expand_more
format_list_bulleted
Concept explainers
Videos
Textbook Question
Chapter 16.5, Problem 16.3CYU
- (a) Which is the stronger Bronsted acid, HCO3− or NH4+? Which has the stronger conjugate base?
- (b) Is a reaction between HCO3- ions and NH3 product- or reactant-favored at equilibrium?
HCO3−(aq) + NH3(aq)
(c) You mix solutions of sodium hydrogen phosphate and ammonia. The net ionic equation for a possible reaction is
HPO42‒(aq) + NH3(aq)
Does the equilibrium lie to the left or to the right for this reaction?
Expert Solution & Answer
Trending nowThis is a popular solution!
Students have asked these similar questions
I would like my graphs checked please. Do they look right? Do I have iodine and persulfate on the right axis ?
Reaction Fill-ins Part 2! Predict the
product(s) OR starting material of the
following reactions. Remember,
Hydride shifts are possible if/when a
more stable carbocation can exist
(depending on reaction mechanism)!
Put your answers in the indicated
boxes d.
d.
ง
HCI
A cylinder contains 12 L of water vapour at 150˚C and 5 atm. The temperature of the water vapour is raised to 175˚C, and the volume of the cylinder is reduced to 8.5 L. What is the final pressure of the gas in atmospheres?
assume that the gas is ideal
Chapter 16 Solutions
Chemistry & Chemical Reactivity
Ch. 16.2 - What are the hydronium ion and hydroxide ion...Ch. 16.4 - For each of the following salts in water, predict...Ch. 16.5 - (a) Which is the stronger Bronsted acid, HCO3 or...Ch. 16.7 - A solution prepared from 0.055 mol of butanoic...Ch. 16.7 - What are the equilibrium concentrations of acetic...Ch. 16.7 - What are the equilibrium concentrations of HF, F...Ch. 16.7 - The weak base, CIO (hypochlorite ion), is used in...Ch. 16.7 - Calculate the pH after mixing 15 mL of 0.12 M...Ch. 16.8 - What is the pH of a 0.10 M solution of oxalic...Ch. 16.10 - Prob. 1.1ACP
Ch. 16.10 - Prob. 1.2ACPCh. 16.10 - The pKa, of the conjugate acid of atropine is...Ch. 16.10 - Convert the pK values to K values for the...Ch. 16.10 - Other solvents also undergo autoionization. (a)...Ch. 16.10 - Prob. 2.3ACPCh. 16.10 - Prob. 2.4ACPCh. 16.10 - To measure the relative strengths of bases...Ch. 16 - Write the formula and the give the name of the...Ch. 16 - Write the formula and give the name of the...Ch. 16 - What are the products of each of the following...Ch. 16 - What are the products of each of the following...Ch. 16 - Write balanced equations showing how the hydrogen...Ch. 16 - Write a balanced equation showing how the HPO42...Ch. 16 - In each of the following acid-base reactions,...Ch. 16 - In each of the following acid-base reactions,...Ch. 16 - An aqueous solution has a pH of 3.75. What is the...Ch. 16 - A saturated solution of milk of magnesia. Mg(OH)2,...Ch. 16 - What is the pH of a 0.0075 M solution of HCl? What...Ch. 16 - What is the pH of a 1.2 104 M solution of KOH?...Ch. 16 - What is the pH of a 0.0015 M solution of Ba(OH)2?Ch. 16 - The pH of a solution of Ba(OH)2 is 10.66 at 25 ....Ch. 16 - Write an equilibrium constant expression for the...Ch. 16 - Write an equilibrium constant expression for the...Ch. 16 - Several acids are listed here with their...Ch. 16 - Several acids are listed here with their...Ch. 16 - Which of the following ions or compounds has the...Ch. 16 - Which of the following compounds or ions has the...Ch. 16 - Which of the following compounds or ions has the...Ch. 16 - Which of the following compounds or ion has the...Ch. 16 - Dissolving K2CO3 in water gives a basic solution....Ch. 16 - Dissolving ammonium bromide in water gives an...Ch. 16 - If each of the salts listed here were dissolved in...Ch. 16 - Which of the following common food additives gives...Ch. 16 - Prob. 27PSCh. 16 - Prob. 28PSCh. 16 - Prob. 29PSCh. 16 - An organic acid has pKa = 8.95. What is its Ka...Ch. 16 - Prob. 31PSCh. 16 - Which is the stronger of the following two acids?...Ch. 16 - Chloroacetic acid (ClCH2CO2H) has Ka = 1.41 103....Ch. 16 - A weak base has Kb = 1.5 109. What is the value...Ch. 16 - The trimethylammonium ion, (CH3)3NH+, is the...Ch. 16 - The chromium(III) ion in water, [Cr(H2O)6]3+. Is a...Ch. 16 - Acetic acid and sodium hydrogen carbonate, NaHCO3,...Ch. 16 - Ammonium chloride and sodium dihydrogen phosphate,...Ch. 16 - For each of the following reactions, predict...Ch. 16 - For each of the following reactions, predict...Ch. 16 - Equal molar quantities of sodium hydroxide and...Ch. 16 - Equal molar quantities of hydrochloric acid and...Ch. 16 - Equal molar quantities of acetic acid and sodium...Ch. 16 - Equal molar quantities of ammonia and sodium...Ch. 16 - A 0.015 M solution of hydrogen cyanate, HOCN, has...Ch. 16 - A 0.10 M solution of chloroacetic acid, CICH2CO2H,...Ch. 16 - A 0.025 M solution of hydroxyl amine has a pH of...Ch. 16 - Methylamine, CH3NH2, is a weak base. CH3NH2(aq) +...Ch. 16 - A 2.5 103 M solution of an unknown acid has a pH...Ch. 16 - A 0.015M solution of a base has a pH of 10.09 a)...Ch. 16 - What are the equilibrium concentrations of...Ch. 16 - The ionizations constant of a very weak acid, HA...Ch. 16 - What are the equilibrium concentration of H3O+, CN...Ch. 16 - Phenol (C6H5OH) commonly called carbolic acid is a...Ch. 16 - What are the equilibrium concentrations of...Ch. 16 - A hypothetical weak base has Kb=5.0104.Calculate...Ch. 16 - The weak base methylamine, CH3NH2, has Kb=4.2104....Ch. 16 - Calculate the pH of a 0.12 M aqueous solution of...Ch. 16 - Calculate the pH of a 0.0010 M aqueous solution of...Ch. 16 - A solution of hydrofluoric acid, HF, has a pH of...Ch. 16 - Calculate the hydronium ion concentration and pH...Ch. 16 - Calculate the hydronium ion concentration and pH...Ch. 16 - Sodium cyanide is the salt of the weak acid HCN....Ch. 16 - The sodium salt of propionic acid, NaCH3CH2CO2 is...Ch. 16 - Calculate the hydronium ion concentration and pH...Ch. 16 - Calculate the hydronium ion concentration and the...Ch. 16 - For each of the following cases, decide whether...Ch. 16 - For each of the following cases, decide whether...Ch. 16 - Oxalic acid, H2C2O4, is a diprotic acid. Write a...Ch. 16 - Sodium carbonate is a diprotic base. Write a...Ch. 16 - Prove that Ka1 Kb2 = Kw for oxalic acid H2C2O4,...Ch. 16 - Prove that Ka3 Kb1 = Kw for phosphoric acid,...Ch. 16 - Sulphurous acid, H2SO3, is a weak acid capable of...Ch. 16 - Ascorbic acid (vitamin C, C6H8O6) is a diprotic...Ch. 16 - Hydrazine, N2H4, can interact with water in two...Ch. 16 - Ethylene diamine, H2NCH2CH2NH2, can interact with...Ch. 16 - Which should be stronger acid, HOCN or HCN?...Ch. 16 - Prob. 78PSCh. 16 - Explain why benzene sulfonic acid is a Brnsted...Ch. 16 - The structure of ethylene diamine is illustrated...Ch. 16 - Decide whether each of the following substances...Ch. 16 - Decide whether each of the following substances...Ch. 16 - Carbon monoxide forms complexes with low-valent...Ch. 16 - Trimethylamine, (CH3)3N, is a common reagent. It...Ch. 16 - About this time, you may be wishing you had an...Ch. 16 - Consider the following ions: NH4+, CO32, Br, S2,...Ch. 16 - A 2.50 g sample of a solid that could be Ba(OH)2...Ch. 16 - In a particular solution, acetic acid is 11%...Ch. 16 - Hydrogen, H2S, and sodium acetate, NaCH3CO2 are...Ch. 16 - For each of the following reactions predict...Ch. 16 - A monoprotic acid HX has Ka = 1.3 103. Calculate...Ch. 16 - Arrange the following 0.10M solutions in order of...Ch. 16 - m-Nitrophenol, a weak acid, can be used as a pH...Ch. 16 - The butylammonium ion, C4H9NH3+, has a Ka of 2.3 ...Ch. 16 - The local anaesthetic novocaine is the hydrogen...Ch. 16 - Pyridine is weak organic base and readily forms a...Ch. 16 - The base ethylamine (CH3CH2NH2) has a Kb of. A...Ch. 16 - Chloroacetic acid, ClCH2CO2H, is a moderately weak...Ch. 16 - Saccharin (HC7H4NO3S) is a weak acid with pKa =...Ch. 16 - Given the following solutions: (a) 0.1 M NH3 (b)...Ch. 16 - For each of the following salts, predict whether a...Ch. 16 - Nicotine, C10H14N2, has two basic nitrogen atoms...Ch. 16 - Prob. 103GQCh. 16 - The equilibrium constant for the reaction of...Ch. 16 - The equilibrium constant for the reaction of...Ch. 16 - Calculate the pH of the solution that results from...Ch. 16 - To what volume should 1.00 102 mL of any weak...Ch. 16 - The hydrogen phthalate ion, C8HsO4, is a weak acid...Ch. 16 - Prob. 109GQCh. 16 - Prob. 110GQCh. 16 - Prob. 111ILCh. 16 - Prob. 112ILCh. 16 - Prob. 113ILCh. 16 - A hydrogen atom in the organic base pyridine,...Ch. 16 - Nicotinic acid, C6H5NO2, is found in minute...Ch. 16 - Prob. 116ILCh. 16 - Sulfanilic acid, which is used in making dyes, is...Ch. 16 - Amino acids are an important group of compounds....Ch. 16 - How can water be both a Brnsied base and a Lewis...Ch. 16 - The nickel(II) ion exists as [Ni(H2O)4]2+ in...Ch. 16 - The halogens form three stable, weak acids, HOX....Ch. 16 - The acidity of the oxoacids was described in...Ch. 16 - Perchloric acid behaves as an acid, even when it...Ch. 16 - You purchase a bottle of water. On checking its...Ch. 16 - Prob. 125SCQCh. 16 - Prob. 126SCQCh. 16 - Prob. 127SCQCh. 16 - Prob. 128SCQCh. 16 - Consider a salt of a weak base and a weak acid...
Knowledge Booster
Learn more about
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
- On the next page is an LC separation of the parabens found in baby wash. Parabens are suspected in a link to breast cancer therefore an accurate way to quantitate them is desired. a. In the chromatogram, estimate k' for ethyl paraben. Clearly indicate what values you used for all the terms in your calculation. b. Is this a "good" value for a capacity factor? Explain. c. What is the resolution between n-Propyl paraben and n-Butyl paraben? Again, indicate clearly what values you used in your calculation. MAU | Methyl paraben 40 20 0 -2 Ethyl paraben n-Propyl paraben n-Butyl paraben App ID 22925 6 8 minarrow_forwardd. In Figure 4, each stationary phase shows some negative correlation between plate count and retention factor. In other words, as k' increases, N decreases. Explain this relationship between k' and N. Plate Count (N) 4000 3500 2500 2000 1500 1000 Figure 4. Column efficiency (N) vs retention factor (k') for 22 nonionizable solutes on FMS (red), PGC (black), and COZ (green). 3000 Eluent compositions (acetonitrile/water, A/W) were adjusted to obtain k' less than 15, which was achieved for most solutes as follows: FMS (30/70 A/W), PGC (60/40), COZ (80/20). Slightly different compositions were used for the most highly retained solutes. All columns were 50 mm × 4.6 mm id and packed with 5 um particles, except for COZ, which was packed with 3 um particles. All other chromatographic conditions were constant: column length 5 cm, column j.§. 4.6 mm, flow rate 2 mL/min, column temperature 40 °C, and injection volume 0.5 μL Log(k'x/K'ethylbenzene) FMS 1.5 1.0 0.5 0.0 ཐྭ ཋ ཤྩ བྷྲ ; 500 0 5 10…arrow_forwardf. Predict how the van Deemter curve in Figure 7 would change if the temperature were raised from 40 °C to 55 °C. Figure 7. van Desmter curves in reduced coordinates for four nitroalkane homologues (nitropropane, black; nitrobutane, red; nitropentane, blue; and nitrohexane, green) separated on the FMS phase. Chromatographic conditions: column dimensions 50 mm × 4.6 mm id, eluent 30/70 ACN/water, flow rates 0.2-5.0 mL/min, injection volume 0.5 and column temperature 40 °C. No corrections to the plate heights have been made to account for extracolumn dispersion. Reduced Plate Height (h) ° 20 40 60 Reduced Velocity (v) 8. (2) A water sample is analyzed for traces of benzene using headspace analysis. The sample and standard are spiked with a fixed amount of toluene as an internal standard. The following data are obtained: Ppb benzene Peak area benzene Peak area toluene 10.0 252 376 Sample 533 368 What is the concentration of benzene in the sample?arrow_forward
- Liquid chromatography has been used to track the concentration of remdesivir (a broad-spectrum antiviral drug, structure shown at right) in COVID patients undergoing experimental treatments. Intensity The authors provide the following details regarding standard solutions preparation: HN CN HO OH NH2 Remdesivir (RDV) stock solution (5000 µg/mL) was prepared by dissolving RDV drug powder using the mixture of DMSO: MeOH (30:70 v/v). The RDV working standard solutions for calibration and quality controls were prepared using methanol in concentrations of 100, 10, 1, 0.1, 0.01 µg/mL. 1, 2.5, 5, 7.5, 10, 25, 50, 75, 100, 250, 500, 1000, and 5000 ng/mL sample solutions were prepared freshly by spiking calibration standard solutions into the blank human plasma samples for method calibration. a) What type of calibration method is being described? Why do you think the authors chose this method as opposed to another? b) Based on the details provided in part a, describe an appropriate method blank…arrow_forwardRecent advancements in liquid chromatography include the development of ultrahigh pressure liquid chromatography (UHPLC) and an increased use of capillary columns that had previously only been used with gas chromatography. Both of these advances have made the development of portable LC systems possible. For example, Axcend Corp. makes a portable system that uses a capillary column with an internal diameter of 150-μm-that is packed with 1.7-um stationary phase particles. In contrast, a traditional LC column has a 4.6 mm internal diameter and utilizes 5-um stationary phase particles. a) Explain one advantage that is afforded by the use of a capillary column in liquid chromatographic separation. Explain one disadvantage of capillary columns. b) Explain how the use of smaller stationary phase particles can improve the resolution of a separation. Include any relevant equations that support your explanation. c) A scientist at Rowan University is using the Axcend LC to conduct analyses of F…arrow_forwardThis paper describes the use of fullerene molecules, also known as buckyballs, as a stationary phase for liquid chromatography. The performance of the fullerene-modified stationary phase (FMS) is compared to that of a more common C18 stationary phase and to two other carbon-based stationary phases, PGC and COZ. A. 10A OM B. - Figure 1. Idealized drawing of the cross-section of a pore inside a silica particle, showing the relative densities of aminopropylsilyl (red/green) and fullerene (blue) groups: (A) full cross- section; (B) detailed view of covalent bonding of fullerene to the silica surface. Surface densities of silyl and fullerene groups were inferred from elemental composition results obtained at each stage of the synthesis (see Table 1). Absorbance (mAU, 220 nm) 700 600 500 400 300 200 100 a. Define selectivity, a, with words and an equation. b. Explain how the choice of stationary phase affects selectivity. c. Calculate the resolution of the nitrobenzene and toluene peaks in…arrow_forward
- Normalized Intensity (a. u.) 0.5 1.0 A 3D-printed GC column (shown below) was created for use with "micro" gas chromatography applications. To prove its utility, it was used to separate a mixture of alkanes (C9-C18, C22, C24). For the separation shown below, the column temperature was ramped from 40 °C to 250 °C at a rate of 30 °C per minute. (a) 9 10 = 1 mm 12 13 15 22 0.0 0 100 200 300 400 Time (sec) a) What detector would you use for this analysis? Justify your selection. b) Explain how the chromatogram would change if the separation was run isothermally. c) Explain how the chromatogram would change if the temperature ramp were increased to 50 °C per minute.arrow_forwardDevise a synthesis of each compound from the indicated starting material. You may also use any organic compounds with one or two carbons and any needed inorganic reagents. a. Brarrow_forwardPlease help me with #2b & #3 using the data.arrow_forward
- Heparin is used as an anti-coagulant. A risk of heparin use is thrombocytopenia, or low platelet count. This risk is minimized with the use of low molecular weight heparins (LMWH), therefore it is desirable to separate LMWH from higher molecular weight heparins. The method of choice to do this is molecular exclusion chromatography. Below is a chromatogram from a molecular exclusion chromatographic run. Peaks ranging from A to J are clearly distinguishable. The heparin mixture that was analyzed had anywhere from 6 to 30 repeat units of monomer (where the heparin with 30 repeat units would be roughly five times the size of the heparin with six repeat units). a. Which letter most likely represents the peak with 6 repeat units given these heparin polymers were separated with molecular exclusion chromatography? b. Explain your reasoning describing the mechanism of retention in molecular exclusion chromatography. 100 80 60 60 Relative Abundance 40 40 E GH 20 20 B A 36 38 40 42 44 46 48 50 50…arrow_forwardHELP NOW PLEASE ! URGENT!arrow_forwardHELP NOW PLEASE ! URGENT!arrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
Chemistry: Principles and PracticeChemistryISBN:9780534420123Author:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward MercerPublisher:Cengage Learning
Chemistry & Chemical ReactivityChemistryISBN:9781337399074Author:John C. Kotz, Paul M. Treichel, John Townsend, David TreichelPublisher:Cengage Learning
Chemistry: Principles and ReactionsChemistryISBN:9781305079373Author:William L. Masterton, Cecile N. HurleyPublisher:Cengage Learning
Chemistry & Chemical ReactivityChemistryISBN:9781133949640Author:John C. Kotz, Paul M. Treichel, John Townsend, David TreichelPublisher:Cengage Learning
ChemistryChemistryISBN:9781305957404Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCostePublisher:Cengage Learning
Chemistry: An Atoms First ApproachChemistryISBN:9781305079243Author:Steven S. Zumdahl, Susan A. ZumdahlPublisher:Cengage Learning
Chemistry: Principles and Practice
Chemistry
ISBN:9780534420123
Author:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward Mercer
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 Reactions
Chemistry
ISBN:9781305079373
Author:William L. Masterton, Cecile N. Hurley
Publisher:Cengage Learning
Chemistry & Chemical Reactivity
Chemistry
ISBN:9781133949640
Author:John C. Kotz, Paul M. Treichel, John Townsend, David Treichel
Publisher:Cengage Learning
Chemistry
Chemistry
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Cengage Learning
Chemistry: An Atoms First Approach
Chemistry
ISBN:9781305079243
Author:Steven S. Zumdahl, Susan A. Zumdahl
Publisher:Cengage Learning
General Chemistry | Acids & Bases; Author: Ninja Nerd;https://www.youtube.com/watch?v=AOr_5tbgfQ0;License: Standard YouTube License, CC-BY