Owlv2 With Ebook, 1 Term (6 Months) Printed Access Card For Kotz/treichel/townsend/treichel's Chemistry & Chemical Reactivity, 10th
10th Edition
ISBN: 9781337791182
Author: John C. Kotz, Paul M. Treichel, John Townsend, David Treichel
Publisher: Cengage Learning
expand_more
expand_more
format_list_bulleted
Question
Chapter 16.10, Problem 2.4ACP
Interpretation Introduction
Interpretation:
A solution of
Concept introduction:
Conductor: It is a type of material and it allows the flow of an
An acid when dissolved in a solution, it has the following properties;
It is a good conductor of electricity.
It changes the color of litmus paper from blue to red.
It tastes sour.
It reacts with a base to produce salt and water.
Non-conductor: It does not conduct the electricity.
Expert Solution & Answer
Want to see the full answer?
Check out a sample textbook solution
Students have asked these similar questions
Draw the less stable chair conformation of myo-inositol clearly indicating the axial and equatorial substituents as well as the cis and trans relationships of at least 3 OH groups.
Draw a viable Newman Projection using any carbon carbon bond clearly showing a gauche interaction between the substituents.
5. What is the product for the following reaction
for each step
and draw the mechanism
H
1. NaNH2
2, EtBr
mical
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…
Chapter 16 Solutions
Owlv2 With Ebook, 1 Term (6 Months) Printed Access Card For Kotz/treichel/townsend/treichel's Chemistry & Chemical Reactivity, 10th
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
Similar questions
- Label these peaks in H- NMR and C- NMRarrow_forwardComplete 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_forward
- Wintergreen 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_forwardSynthesis 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_forward
- Acid 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_forwardAssign this H NMRarrow_forwardPlease complete these blanks need that asaparrow_forward
- Nitration 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_forwardSodium Borohydride Reduction (continued on the next page): 1. Draw the product of each of the reactions below and give the formula mass to the nearest whole number. ? (1) NaBH (2) acid (1) NaBD4 (2) acid ? 2. In mass spectra, alcohols typically break as shown in equation 8 in chapter 11 (refer to your lab manual). The larger group is generally lost and this gives rise to the base peak in the mass spectrum. For the products of each of the reactions in question # 1, draw the ion corresponding to the base peak for that product and give its mass to charge ratio (m/z). 3. Given the reaction below, calculate how many mg of 1-phenyl-1-butanol that can be produced using 31 mg NaBH4 and an excess of butyrophenone. 4. + NaBH4 OH (after workup with dilute HCI) 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_forwardAspirin from Wintergreen: 1. In isolating the salicylic acid, why is it important to press out as much of the water as possible? Write a step-by-step mechanism for the esterification of salicylic acid with acetic anhydride catalyzed by concentrated H₂SO4. 3. Calculate the exact monoisotopic mass of aspirin showing your work. 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
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
Chemistry & Chemical ReactivityChemistryISBN:9781337399074Author:John C. Kotz, Paul M. Treichel, John Townsend, David TreichelPublisher:Cengage Learning
Chemistry: Principles and PracticeChemistryISBN:9780534420123Author:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward MercerPublisher:Cengage Learning
Chemistry: The Molecular ScienceChemistryISBN:9781285199047Author:John W. Moore, Conrad L. StanitskiPublisher: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 & 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
Chemistry: The Molecular Science
Chemistry
ISBN:9781285199047
Author:John W. Moore, Conrad L. Stanitski
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