Interpretation:
Amount of HCl in solution is to be calculated.
Concept introduction:
Dilution is the process of decreasing the concentration of a stock solution by adding more solvent to the solution. The solvent added is usually the universal solvent, known as water. The more solvent you add, the more diluted the solution will get.
In dilution, the amount of solute does not change, the number of moles is the same before and after dilution.
If subscript "1" represents initial and "2" represents the final values of the quantities involved, we have:
Here, molarity is used as a unit of concentration and n1 and n2 are the number of moles before and after dilution respectively.
n1 = n2 and thus,
The equation for dilution is
Where
M1 = molarity of the stock solution
V1 = volume of stock solution
M2 = molarity of the diluted solution
V2 = volume of diluted solution

Answer to Problem 26PP
91.15 gmHCl is present in the solution.
As we know, in dilution, the amount of solute does not change, the number of moles is the same before and after dilution.
Here, the equation is requiredn1 = M1V1
M1 = molarity of the stock solution V1 = volume of stock solution
Data Given: M1 = molarity of the stock solution = 5.0 M
V1 = volume of stock HCl solution = 0.5 L
n1 = M1V1
= 5.0 M × 0.5 L = 2.5 mol Number of moles of HCl
Calculate the mass of HCl from above equation:
Thus, 91.15 gmHCl is present in the solution.
Explanation of Solution
As we know, in dilution, the amount of solute does not change, the number of moles is the same before and after dilution.
Here, the equation is requiredn1 = M1V1
M1 = molarity of the stock solution V1 = volume of stock solution
Data Given: M1 = molarity of the stock solution = 5.0 M
V1 = volume of stock HCl solution = 0.5 L
n1 = M1V1
= 5.0 M × 0.5 L = 2.5 mol Number of moles of HCl
Calculate the mass of HCl from above equation:
Thus, 91.15 gmHCl is present in the solution.
Chapter 14 Solutions
Chemistry: Matter and Change
Additional Science Textbook Solutions
Campbell Biology: Concepts & Connections (9th Edition)
Human Physiology: An Integrated Approach (8th Edition)
Chemistry: The Central Science (14th Edition)
Campbell Biology in Focus (2nd Edition)
Campbell Biology (11th Edition)
College Physics: A Strategic Approach (3rd Edition)
- Draw a Haworth projection of a common cyclic form of this monosaccharide: H HO H HO H HO H H -OH CH2OH Click and drag to start drawing a structure. Х : Darrow_forward: Draw the structure of valylasparagine, a dipeptide made from valine and asparagine, as it would appear at physiological pH. Click and drag to start drawing a structure. P Darrow_forwardDraw the Haworth projection of α-L-mannose. You will find helpful information in the ALEKS Data resource. Click and drag to start drawing a structure. : ཊི Х Darrow_forward
- Draw the structure of serine at pH 6.8. Click and drag to start drawing a structure. : d كarrow_forwardTake a look at this molecule, and then answer the questions in the table below it. CH2OH H H H OH OH OH CH2OH H H H H OH H H OH H OH Is this a reducing sugar? yes α β ロ→ロ no ☑ yes Does this molecule contain a glycosidic bond? If you said this molecule does contain a glycosidic bond, write the symbol describing it. O no 0+0 If you said this molecule does contain a glycosidic bond, write the common names (including anomer and enantiomer labels) of the molecules that would be released if that bond were hydrolyzed. If there's more than one molecule, separate each name with a comma. ☐arrow_forwardAnswer the questions in the table below about this molecule: H₂N-CH₂ -C—NH–CH–C—NH–CH—COO- CH3 CH CH3 What kind of molecule is this? 0= CH2 C If you said the molecule is a peptide, write a description of it using 3-letter codes separated ☐ by dashes. polysaccharide peptide amino acid phospolipid none of the above Хarrow_forward
- Draw a Haworth projection of a common cyclic form of this monosaccharide: CH₂OH C=O HO H H -OH H OH CH₂OH Click and drag to start drawing a structure. : ☐ Х S '☐arrow_forwardNucleophilic Aromatic Substitution 22.30 Predict all possible products formed from the following nucleophilic substitution reactions. (a) (b) 9 1. NaOH 2. HCI, H₂O CI NH₁(!) +NaNH, -33°C 1. NaOH 2. HCl, H₂Oarrow_forwardSyntheses 22.35 Show how to convert toluene to these compounds. (a) -CH,Br (b) Br- -CH3 22.36 Show how to prepare each compound from 1-phenyl-1-propanone. 1-Phenyl-1-propanone ہتی. Br. (b) Br (racemic) 22.37 Show how to convert ethyl benzene to (a) 2,5-dichlorobenzoic acid and (b) 2,4-dichlorobenzoic acid. 22.38 Show reagents and conditions to bring about the following conversions. (a) 9 NH2 8 CO₂H NH2 CO₂Et (d) NO2 NH2 S NH₂ NO2 CHS CHarrow_forward
- ive the major organic product(s) of each of the following reactions or sequences of reactions. Show all rant stereochemistry. [10 only] A. B. NaN3 1. LiAlH4, ether Br 2. H₂O CH3 HNO3 H₂/Pt H₂SO ethanol C. 0 0 CH3CC1 NaOH NHCCH AICI H₂O . NH₂ CH3CH2 N CH2CH3 + HCI CH₂CH 3 1. LIAIH, THE 2. H₂Oarrow_forwardCalculate the stoichiometric amount of CaCl2 needed to convert all of the CuSO4 into CuCl2.arrow_forwardH CH تنی Cl 1. NaCN, DMF 2. LIAIH4, ether H₂O pyridine N NH₂ 5 CH H 1 HNO, H₂SO 2. Nal NH2 Br Br HNO₂ CuCl H₂SO HCI CH3 H3C NN HSO KCN CuCN 1. HNO₂, H₂SO O₂N NH2 2. OH ཀ་ལས། །ས་ཅན་ :i་དེ་མ་མ་སེ་ NH₂ CH3 1. HNO₂, H₂SO4 2. H3PO₂ 1 HNO2, H2SO4 2. Nalarrow_forward
- ChemistryChemistryISBN:9781305957404Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCostePublisher:Cengage LearningChemistryChemistryISBN:9781259911156Author:Raymond Chang Dr., Jason Overby ProfessorPublisher:McGraw-Hill EducationPrinciples of Instrumental AnalysisChemistryISBN:9781305577213Author:Douglas A. Skoog, F. James Holler, Stanley R. CrouchPublisher:Cengage Learning
- Organic ChemistryChemistryISBN:9780078021558Author:Janice Gorzynski Smith Dr.Publisher:McGraw-Hill EducationChemistry: Principles and ReactionsChemistryISBN:9781305079373Author:William L. Masterton, Cecile N. HurleyPublisher:Cengage LearningElementary Principles of Chemical Processes, Bind...ChemistryISBN:9781118431221Author:Richard M. Felder, Ronald W. Rousseau, Lisa G. BullardPublisher:WILEY





