ACHIEVE/CHEMICAL PRINCIPLES ACCESS 1TERM
7th Edition
ISBN: 9781319399849
Author: ATKINS
Publisher: MAC HIGHER
expand_more
expand_more
format_list_bulleted
Concept explainers
Question
Chapter 6, Problem 6C.3AST
(a)
Interpretation Introduction
Interpretation:
Stronger acid has to be predicted among
Concept Introduction:
Strength of acid can be predicted using the following points;
- Electronegativity of halogen if present in the oxoacid, the strength of oxoacid will be more.
- If more number of oxygen atoms is bonded to the central atom, then the acid will be stronger.
- If the oxidation state of the central atom is more, then the acid will be stronger.
(b)
Interpretation Introduction
Interpretation:
Stronger acid has to be predicted among
Concept Introduction:
Refer part (a).
(c)
Interpretation Introduction
Interpretation:
Stronger acid has to be predicted among
Concept Introduction:
Refer part (a).
Expert Solution & Answer
Want to see the full answer?
Check out a sample textbook solutionStudents have asked these similar questions
Predict whether aqueous solutions of the following substances are acidic, basic, or neutral and write hydrolysis equations for the acidic and basic solutions.
(a) CsBr; (b) Al(NO3)3; (c) KCN; (d) CH3NH3Cl
(a) Given that Ka for acetic acid is 1.8 x 10-5 and that hypochlorous acid is 3.0 x10-8 , which is a stronger acid?
(b) Which is the stronger base, the acetate ion or the hypochlorite ion?
(c) calculate the Kb values for the CHCOO- and ClO- .
For the following acid-base reaction, (1) predict the products, showing both reactants and products
complete Lewis structures and arrows showing electron flow; (2) label each structure with the
lowing: Bronsted acid, Bronsted base, conjugate acid, conjugate base; (3) give a brief definition of a
ronsted acid and Bronsted base; (4) predict the direction of the equilibrium and justify your answer.
HC0OH + CH3 Nta
PRん106Y
pkb = 3.36
Chapter 6 Solutions
ACHIEVE/CHEMICAL PRINCIPLES ACCESS 1TERM
Ch. 6 - Prob. 6A.1ASTCh. 6 - Prob. 6A.1BSTCh. 6 - Prob. 6A.2ASTCh. 6 - Prob. 6A.2BSTCh. 6 - Prob. 6A.3ASTCh. 6 - Prob. 6A.3BSTCh. 6 - Prob. 6A.1ECh. 6 - Prob. 6A.2ECh. 6 - Prob. 6A.3ECh. 6 - Prob. 6A.4E
Ch. 6 - Prob. 6A.5ECh. 6 - Prob. 6A.6ECh. 6 - Prob. 6A.7ECh. 6 - Prob. 6A.8ECh. 6 - Prob. 6A.9ECh. 6 - Prob. 6A.10ECh. 6 - Prob. 6A.11ECh. 6 - Prob. 6A.12ECh. 6 - Prob. 6A.13ECh. 6 - Prob. 6A.14ECh. 6 - Prob. 6A.15ECh. 6 - Prob. 6A.16ECh. 6 - Prob. 6A.17ECh. 6 - Prob. 6A.18ECh. 6 - Prob. 6A.19ECh. 6 - Prob. 6A.20ECh. 6 - Prob. 6A.21ECh. 6 - Prob. 6A.22ECh. 6 - Prob. 6A.23ECh. 6 - Prob. 6A.24ECh. 6 - Prob. 6B.1ASTCh. 6 - Prob. 6B.1BSTCh. 6 - Prob. 6B.2ASTCh. 6 - Prob. 6B.2BSTCh. 6 - Prob. 6B.3ASTCh. 6 - Prob. 6B.3BSTCh. 6 - Prob. 6B.1ECh. 6 - Prob. 6B.2ECh. 6 - Prob. 6B.3ECh. 6 - Prob. 6B.4ECh. 6 - Prob. 6B.5ECh. 6 - Prob. 6B.6ECh. 6 - Prob. 6B.7ECh. 6 - Prob. 6B.8ECh. 6 - Prob. 6B.9ECh. 6 - Prob. 6B.10ECh. 6 - Prob. 6B.11ECh. 6 - Prob. 6B.12ECh. 6 - Prob. 6C.1ASTCh. 6 - Prob. 6C.1BSTCh. 6 - Prob. 6C.2ASTCh. 6 - Prob. 6C.2BSTCh. 6 - Prob. 6C.3ASTCh. 6 - Prob. 6C.3BSTCh. 6 - Prob. 6C.1ECh. 6 - Prob. 6C.2ECh. 6 - Prob. 6C.3ECh. 6 - Prob. 6C.4ECh. 6 - Prob. 6C.5ECh. 6 - Prob. 6C.6ECh. 6 - Prob. 6C.7ECh. 6 - Prob. 6C.8ECh. 6 - Prob. 6C.9ECh. 6 - Prob. 6C.10ECh. 6 - Prob. 6C.11ECh. 6 - Prob. 6C.12ECh. 6 - Prob. 6C.13ECh. 6 - Prob. 6C.14ECh. 6 - Prob. 6C.15ECh. 6 - Prob. 6C.16ECh. 6 - Prob. 6C.17ECh. 6 - Prob. 6C.18ECh. 6 - Prob. 6C.19ECh. 6 - Prob. 6C.20ECh. 6 - Prob. 6C.21ECh. 6 - Prob. 6C.22ECh. 6 - Prob. 6D.1ASTCh. 6 - Prob. 6D.1BSTCh. 6 - Prob. 6D.2ASTCh. 6 - Prob. 6D.2BSTCh. 6 - Prob. 6D.3ASTCh. 6 - Prob. 6D.3BSTCh. 6 - Prob. 6D.4ASTCh. 6 - Prob. 6D.4BSTCh. 6 - Prob. 6D.5ASTCh. 6 - Prob. 6D.5BSTCh. 6 - Prob. 6D.6ASTCh. 6 - Prob. 6D.6BSTCh. 6 - Prob. 6D.1ECh. 6 - Prob. 6D.2ECh. 6 - Prob. 6D.3ECh. 6 - Prob. 6D.4ECh. 6 - Prob. 6D.5ECh. 6 - Prob. 6D.6ECh. 6 - Prob. 6D.7ECh. 6 - Prob. 6D.8ECh. 6 - Prob. 6D.9ECh. 6 - Prob. 6D.11ECh. 6 - Prob. 6D.12ECh. 6 - Prob. 6D.13ECh. 6 - Prob. 6D.14ECh. 6 - Prob. 6D.15ECh. 6 - Prob. 6D.16ECh. 6 - Prob. 6D.17ECh. 6 - Prob. 6D.18ECh. 6 - Prob. 6D.19ECh. 6 - Prob. 6D.20ECh. 6 - Prob. 6D.21ECh. 6 - Prob. 6D.22ECh. 6 - Prob. 6E.1ASTCh. 6 - Prob. 6E.1BSTCh. 6 - Prob. 6E.2ASTCh. 6 - Prob. 6E.2BSTCh. 6 - Prob. 6E.3ASTCh. 6 - Prob. 6E.1ECh. 6 - Prob. 6E.2ECh. 6 - Prob. 6E.3ECh. 6 - Prob. 6E.4ECh. 6 - Prob. 6E.5ECh. 6 - Prob. 6E.6ECh. 6 - Prob. 6E.7ECh. 6 - Prob. 6E.8ECh. 6 - Prob. 6E.9ECh. 6 - Prob. 6E.10ECh. 6 - Prob. 6E.11ECh. 6 - Prob. 6E.12ECh. 6 - Prob. 6E.13ECh. 6 - Prob. 6E.14ECh. 6 - Prob. 6E.15ECh. 6 - Prob. 6E.16ECh. 6 - Prob. 6E.17ECh. 6 - Prob. 6E.18ECh. 6 - Prob. 6F.1ASTCh. 6 - Prob. 6F.1BSTCh. 6 - Prob. 6F.2ASTCh. 6 - Prob. 6F.2BSTCh. 6 - Prob. 6F.1ECh. 6 - Prob. 6F.2ECh. 6 - Prob. 6F.3ECh. 6 - Prob. 6F.4ECh. 6 - Prob. 6F.5ECh. 6 - Prob. 6F.6ECh. 6 - Prob. 6F.7ECh. 6 - Prob. 6F.9ECh. 6 - Prob. 6F.10ECh. 6 - Prob. 6G.1ASTCh. 6 - Prob. 6G.1BSTCh. 6 - Prob. 6G.2ASTCh. 6 - Prob. 6G.2BSTCh. 6 - Prob. 6G.3ASTCh. 6 - Prob. 6G.3BSTCh. 6 - Prob. 6G.4ASTCh. 6 - Prob. 6G.4BSTCh. 6 - Prob. 6G.1ECh. 6 - Prob. 6G.3ECh. 6 - Prob. 6G.4ECh. 6 - Prob. 6G.5ECh. 6 - Prob. 6G.6ECh. 6 - Prob. 6G.7ECh. 6 - Prob. 6G.8ECh. 6 - Prob. 6G.9ECh. 6 - Prob. 6G.11ECh. 6 - Prob. 6G.12ECh. 6 - Prob. 6G.13ECh. 6 - Prob. 6G.14ECh. 6 - Prob. 6G.15ECh. 6 - Prob. 6G.16ECh. 6 - Prob. 6G.19ECh. 6 - Prob. 6G.20ECh. 6 - Prob. 6H.1ASTCh. 6 - Prob. 6H.1BSTCh. 6 - Prob. 6H.2ASTCh. 6 - Prob. 6H.2BSTCh. 6 - Prob. 6H.3ASTCh. 6 - Prob. 6H.3BSTCh. 6 - Prob. 6H.4ASTCh. 6 - Prob. 6H.4BSTCh. 6 - Prob. 6H.5ASTCh. 6 - Prob. 6H.5BSTCh. 6 - Prob. 6H.1ECh. 6 - Prob. 6H.3ECh. 6 - Prob. 6H.9ECh. 6 - Prob. 6H.10ECh. 6 - Prob. 6H.15ECh. 6 - Prob. 6H.16ECh. 6 - Prob. 6H.21ECh. 6 - Prob. 6H.22ECh. 6 - Prob. 6H.23ECh. 6 - Prob. 6H.24ECh. 6 - Prob. 6H.25ECh. 6 - Prob. 6H.26ECh. 6 - Prob. 6H.27ECh. 6 - Prob. 6H.28ECh. 6 - Prob. 6H.29ECh. 6 - Prob. 6H.30ECh. 6 - Prob. 6H.31ECh. 6 - Prob. 6H.32ECh. 6 - Prob. 6I.1ASTCh. 6 - Prob. 6I.1BSTCh. 6 - Prob. 6I.2ASTCh. 6 - Prob. 6I.2BSTCh. 6 - Prob. 6I.3ASTCh. 6 - Prob. 6I.3BSTCh. 6 - Prob. 6I.4ASTCh. 6 - Prob. 6I.4BSTCh. 6 - Prob. 6I.1ECh. 6 - Prob. 6I.2ECh. 6 - Prob. 6I.3ECh. 6 - Prob. 6I.4ECh. 6 - Prob. 6I.5ECh. 6 - Prob. 6I.6ECh. 6 - Prob. 6I.7ECh. 6 - Prob. 6I.8ECh. 6 - Prob. 6I.9ECh. 6 - Prob. 6I.10ECh. 6 - Prob. 6I.11ECh. 6 - Prob. 6I.12ECh. 6 - Prob. 6J.1ASTCh. 6 - Prob. 6J.1BSTCh. 6 - Prob. 6J.2ASTCh. 6 - Prob. 6J.2BSTCh. 6 - Prob. 6J.1ECh. 6 - Prob. 6J.2ECh. 6 - Prob. 6J.3ECh. 6 - Prob. 6J.4ECh. 6 - Prob. 6J.9ECh. 6 - Prob. 6J.10ECh. 6 - Prob. 6J.11ECh. 6 - Prob. 6J.15ECh. 6 - Prob. 6J.17ECh. 6 - Prob. 6K.1ASTCh. 6 - Prob. 6K.1BSTCh. 6 - Prob. 6K.2ASTCh. 6 - Prob. 6K.2BSTCh. 6 - Prob. 6K.1ECh. 6 - Prob. 6K.2ECh. 6 - Prob. 6K.3ECh. 6 - Prob. 6K.4ECh. 6 - Prob. 6K.5ECh. 6 - Prob. 6K.6ECh. 6 - Prob. 6K.7ECh. 6 - Prob. 6K.8ECh. 6 - Prob. 6L.1ASTCh. 6 - Prob. 6L.1BSTCh. 6 - Prob. 6L.2ASTCh. 6 - Prob. 6L.2BSTCh. 6 - Prob. 6L.3ASTCh. 6 - Prob. 6L.3BSTCh. 6 - Prob. 6L.1ECh. 6 - Prob. 6L.2ECh. 6 - Prob. 6L.3ECh. 6 - Prob. 6L.4ECh. 6 - Prob. 6L.5ECh. 6 - Prob. 6L.7ECh. 6 - Prob. 6L.9ECh. 6 - Prob. 6M.1ASTCh. 6 - Prob. 6M.1BSTCh. 6 - Prob. 6M.2ASTCh. 6 - Prob. 6M.2BSTCh. 6 - Prob. 6M.3ASTCh. 6 - Prob. 6M.3BSTCh. 6 - Prob. 6M.4ASTCh. 6 - Prob. 6M.4BSTCh. 6 - Prob. 6M.1ECh. 6 - Prob. 6M.2ECh. 6 - Prob. 6M.9ECh. 6 - Prob. 6M.10ECh. 6 - Prob. 6N.1ASTCh. 6 - Prob. 6N.1BSTCh. 6 - Prob. 6N.2ASTCh. 6 - Prob. 6N.2BSTCh. 6 - Prob. 6N.3BSTCh. 6 - Prob. 6N.4ASTCh. 6 - Prob. 6N.4BSTCh. 6 - Prob. 6N.1ECh. 6 - Prob. 6N.2ECh. 6 - Prob. 6N.5ECh. 6 - Prob. 6N.6ECh. 6 - Prob. 6N.7ECh. 6 - Prob. 6N.9ECh. 6 - Prob. 6N.10ECh. 6 - Prob. 6N.11ECh. 6 - Prob. 6N.12ECh. 6 - Prob. 6N.21ECh. 6 - Prob. 6N.23ECh. 6 - Prob. 6O.1ASTCh. 6 - Prob. 6O.1BSTCh. 6 - Prob. 6O.2ASTCh. 6 - Prob. 6O.2BSTCh. 6 - Prob. 6O.3ASTCh. 6 - Prob. 6O.3BSTCh. 6 - Prob. 6O.4ASTCh. 6 - Prob. 6O.4BSTCh. 6 - Prob. 6O.1ECh. 6 - Prob. 6O.2ECh. 6 - Prob. 6O.3ECh. 6 - Prob. 6O.4ECh. 6 - Prob. 6O.5ECh. 6 - Prob. 6O.6ECh. 6 - Prob. 6O.7ECh. 6 - Prob. 6O.8ECh. 6 - Prob. 6O.9ECh. 6 - Prob. 6O.10ECh. 6 - Prob. 6O.11ECh. 6 - Prob. 6O.12ECh. 6 - Prob. 6O.13ECh. 6 - Prob. 6O.14ECh. 6 - Prob. 6O.15ECh. 6 - Prob. 6O.16ECh. 6 - Prob. 6.1ECh. 6 - Prob. 6.3ECh. 6 - Prob. 6.4ECh. 6 - Prob. 6.5ECh. 6 - Prob. 6.6ECh. 6 - Prob. 6.8ECh. 6 - Prob. 6.9ECh. 6 - Prob. 6.10ECh. 6 - Prob. 6.11ECh. 6 - Prob. 6.12ECh. 6 - Prob. 6.13ECh. 6 - Prob. 6.14ECh. 6 - Prob. 6.25ECh. 6 - Prob. 6.40ECh. 6 - Prob. 6.41ECh. 6 - Prob. 6.43ECh. 6 - Prob. 6.45ECh. 6 - Prob. 6.46ECh. 6 - Prob. 6.47ECh. 6 - Prob. 6.51ECh. 6 - Prob. 6.53ECh. 6 - Prob. 6.65ECh. 6 - Prob. 6.75ECh. 6 - Prob. 6.77E
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
- For conjugate acidbase pairs, how are Ka and Kb related? Consider the reaction of acetic acid in water CH3CO2H(aq)+H2O(l)CH3CO2(aq)+H3O+(aq) where Ka = 1.8 105 a. Which two bases are competing for the proton? b. Which is the stronger base? c. In light of your answer to part b. why do we classify the acetate ion (CH3CO2) as a weak base? Use an appropriate reaction to justify your answer. In general, as base strength increases, conjugate acid strength decreases. Explain why the conjugate acid of the weak base NH3 is a weak acid. To summarize, the conjugate base of a weak acid is a weak base and the conjugate acid of a weak base is a weak acid (weak gives you weak). Assuming Ka for a monoprotic strong acid is 1 106, calculate Kb for the conjugate base of this strong acid. Why do conjugate bases of strong acids have no basic properties in water? List the conjugate bases of the six common strong acids. To tie it all together, some instructors have students think of Li+, K+, Rb+, Cs+, Ca2+, Sr2+, and Ba2+ as the conjugate acids of the strong bases LiOH, KOH. RbOH, CsOH, Ca(OH)2, Sr(OH)2, and Ba(OH)2. Although not technically correct, the conjugate acid strength of these cations is similar to the conjugate base strength of the strong acids. That is, these cations have no acidic properties in water; similarly, the conjugate bases of strong acids have no basic properties (strong gives you worthless). Fill in the blanks with the correct response. The conjugate base of a weak acid is a_____base. The conjugate acid of a weak base is a_____acid. The conjugate base of a strong acid is a_____base. The conjugate acid of a strong base is a_____ acid. (Hint: Weak gives you weak and strong gives you worthless.)arrow_forwardThe sec-butyl cation can react as both a Brnsted-Lowry acid (a proton donor) and a Lewis acid (an electron pair acceptor) in the presence of a watersulfuric acid mixture. In each case, however, the product is different. The two reactions are as follows: (a) In which reaction(s) does this cation react as a Lewis acid? In which reaction(s) does it react as a Brnsted-Lowry acid? (b) Write Lewis structures for reactants and products and show by the use of curved arrows how each reaction occurs.arrow_forwardThe following reactions illustrate Brnsted acid-base behavior. Complete each equation. a.HI(aq)+?H3O+(aq)+I(aq) b.NH3(l)+?NH4++NH2 c.H2C2O4(aq)+H2O(l)?+HC2O4(aq) d.H2N2O2(aq)+H2O(l)H3O+(aq)+? e.?+H2O(l)H3O+(aq)+CO32(aq)arrow_forward
- Weak base B has a pKb of 6.78 and weak acid HA has a pKa of 5.12. a Which is the stronger base, B or A? b Which is the stronger acid, HA or BH+? c Consider the following reaction: B(aq)+HA(aq)BH+(aq)+A(aq) Based on the information about the acid/base strengths for the species in this reaction, is this reaction favored to proceed more to the right or more to the left? Why? d An aqueous solution is made in which the concentration of weak base B is one half the concentration of its acidic salt, BHCl, where BH+ is the conjugate weak add of B. Calculate the pH of the solution. e An aqueous solution is made in which the concentration of weak acid HA twice the concentration of the sodium salt of the weak acid, NaA. Calculate the pH of the solution. f Assume the conjugate pairs B/BH+ and HA/A are capable of being used as color-based end point indicators in acidbase titrations, where B is the base form indicator and BH is the acid form indicator, and HA is the acid form indicator and A is the base form indicator. Select the indicator pair that would be best to use in each of the following titrations: (1) Titration of a strong acid with a strong base. (i) B/BH+ (ii) HA/A (2) Titration of a weak base with a strong acid. (i) B/BH+ (ii) HA/Aarrow_forwardConsider these acids (a) Arrange the acids in order of increasing acid strength from weakest to strongest. (b) Which acid has the smallest pKa value?arrow_forwardAcid-Base Equilibria Many factors contribute to the acidity of organic compounds. Electronegativity, resonance, induction, hybridization, aromaticity, and atomic size, all play a role. In the following comparisons, you are asked to identify the factor(s) that would be most important to analyze when predicting relative acidity, and then to predict the trend in acidity and pKa values. For each of the following pairs of compounds answer the following two multiple-choice questions. 1. What factor(s) are the most important to consider when predicting the relative acidity of the two compounds? a. Electronegativity of the atom possessing the hydrogen. b. Resonance stabilization of the anionic conjugate base. c. Inductive stabilization of the anionic conjugate base. d. Hybridization of the atom possessing the hydrogen. e. The atomic size of the atom possessing the hydrogen.arrow_forward
- Calculate the equilibrium constant for the acid–base reaction between the reactants in each of the following pairs: (a) HCl + H2O (b) CH3COOH + H2O (c) CH3NH2 + H2O (d) CH3N+H3 + H2Oarrow_forwardIn the following reactions, identify the Lewis acid and the Lewis base. (a) AlCl3 + Cl¯ → AICI, (b) CH;COOH(aq) + NH3(aq) → CH;COO (aq) + NH (aq) (c) Co³* (aq) + 6F (aq) → [CoF, j*¯ (aq)arrow_forwardConsider the base hydroxylamine, NH2OH. (a) What is theconjugate acid of hydroxylamine? (b) When it acts as a base,which atom in hydroxylamine accepts a proton? (c) Thereare two atoms in hydroxylamine that have nonbondingelectron pairs that could act as proton acceptors. Use Lewisstructures and formal charges to rationalizewhy one of these two atoms is a much better proton acceptorthan the other.arrow_forward
- Consider the following bases: A Which of the following statements is true? (i) The ions increase in basicity as follows: A < B < C, with C being the strongest base. (ii) The conjugate acid of C would have the highest pKa of the conjugate acids of the three bases. (iii) A is the best electron donor. O ii only O i only O two of i, ii and i O i only O None of i, ii and iiiarrow_forwardWhich is the stronger base, (CH3)3N or H2 BO3− ?arrow_forwardWrite complete Lewis structures of the molecules in the following reactions. Which is the Lewis acid and which the Lewis base in each reaction? a)H3N + AlH3➞ H3N–AlH3 b)CS2 + SH–➞ HCS3–arrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
- Chemistry & Chemical ReactivityChemistryISBN:9781133949640Author:John C. Kotz, Paul M. Treichel, John Townsend, David TreichelPublisher:Cengage LearningChemistry for Today: General, Organic, and Bioche...ChemistryISBN:9781305960060Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. HansenPublisher:Cengage LearningOrganic Chemistry: A Guided InquiryChemistryISBN:9780618974122Author:Andrei StraumanisPublisher:Cengage Learning
- Chemistry: Principles and ReactionsChemistryISBN:9781305079373Author:William L. Masterton, Cecile N. HurleyPublisher:Cengage LearningChemistry: Principles and PracticeChemistryISBN:9780534420123Author:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward MercerPublisher:Cengage LearningChemistry: Matter and ChangeChemistryISBN:9780078746376Author:Dinah Zike, Laurel Dingrando, Nicholas Hainen, Cheryl WistromPublisher:Glencoe/McGraw-Hill School Pub Co
Chemistry & Chemical Reactivity
Chemistry
ISBN:9781133949640
Author:John C. Kotz, Paul M. Treichel, John Townsend, David Treichel
Publisher:Cengage Learning
Chemistry for Today: General, Organic, and Bioche...
Chemistry
ISBN:9781305960060
Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. Hansen
Publisher:Cengage Learning
Organic Chemistry: A Guided Inquiry
Chemistry
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Cengage Learning
Chemistry: Principles and Reactions
Chemistry
ISBN:9781305079373
Author:William L. Masterton, Cecile N. Hurley
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: Matter and Change
Chemistry
ISBN:9780078746376
Author:Dinah Zike, Laurel Dingrando, Nicholas Hainen, Cheryl Wistrom
Publisher:Glencoe/McGraw-Hill School Pub Co
ENVIRONMENTAL POLLUTION; Author: 7activestudio;https://www.youtube.com/watch?v=oxtMFmDTv3Q;License: Standard YouTube License, CC-BY