Concept explainers
(a)
Interpretation:
Stronger acid in the given pair of
Concept introduction:
Increasing acid strength:
Acids strength is mainly depending on the dissociation of ions, strong acids dissociates completely and weak acid dissociate slightly.
The hydrohalic acids are strong acids (
Oxoacids are strong acid when the number of oxygen excess than the ionizable proton by two or more oxygen atom for example,
The hydrogen atom which is not bonded to halogen atom or oxygen atoms are weak acid for example
The number of protons is equal to number oxygen in Oxoacids are weak acid for example
The acid strength is depending on the
Acid Strength of Nonmetal Hydrides:
The acid strength is increases across a period, the acid strength is increases down a group.
Electronegativity:
It is the ability of atom to attract a lone pair of electrons towards itself in a substrate. Electronegativity property follows the trend that it increases across the periods and decreases down the column in the periodic table.
(b)
Interpretation:
Stronger acid in the given pair of
Concept introduction:
Increasing acid strength:
Acids strength is mainly depending on the dissociation of ions, strong acids dissociates completely and weak acid dissociate slightly.
The hydrohalic acids are strong acids (
Oxoacids are strong acid when the number of oxygen excess than the ionizable proton by two or more oxygen atom for example,
The hydrogen atom which is not bonded to halogen atom or oxygen atoms are weak acid for example
The number of protons is equal to number oxygen in Oxoacids are weak acid for example
The acid strength is depending on the
Acid Strength of Nonmetal Hydrides:
The acid strength is increases across a period, the acid strength is increases down a group.
Electronegativity:
It is the ability of atom to attract a lone pair of electrons towards itself in a substrate. Electronegativity property follows the trend that it increases across the periods and decreases down the column in the periodic table.
(c)
Interpretation:
Stronger acid in the given pair of
Concept introduction:
Increasing acid strength:
Acids strength is mainly depending on the dissociation of ions, strong acids dissociates completely and weak acid dissociate slightly.
The hydrohalic acids are strong acids (
Oxoacids are strong acid when the number of oxygen excess than the ionizable proton by two or more oxygen atom for example,
The hydrogen atom which is not bonded to halogen atom or oxygen atoms are weak acid for example
The number of protons is equal to number oxygen in Oxoacids are weak acid for example
The acid strength is depending on the
Acid Strength of Nonmetal Hydrides:
The acid strength is increases across a period, the acid strength is increases down a group.
Electronegativity:
It is the ability of atom to attract a lone pair of electrons towards itself in a substrate. Electronegativity property follows the trend that it increases across the periods and decreases down the column in the periodic table.
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Chapter 18 Solutions
CHEMISTRY: MOLECULAR NATURE OF MATTER
- Diels Alder Cycloaddition: Focus on regiochemistry (problems E-F) –> match + of thedienophile and - of the diene while also considering stereochemistry (endo).arrow_forwardHELP! URGENT! PLEASE RESOND ASAP!arrow_forwardQuestion 4 Determine the rate order and rate constant for sucrose hydrolysis. Time (hours) [C6H12O6] 0 0.501 0.500 0.451 1.00 0.404 1.50 0.363 3.00 0.267 First-order, k = 0.210 hour 1 First-order, k = 0.0912 hour 1 O Second-order, k = 0.590 M1 hour 1 O Zero-order, k = 0.0770 M/hour O Zero-order, k = 0.4896 M/hour O Second-order, k = 1.93 M-1-hour 1 10 ptsarrow_forward
- Determine the rate order and rate constant for sucrose hydrolysis. Time (hours) [C6H12O6] 0 0.501 0.500 0.451 1.00 0.404 1.50 0.363 3.00 0.267arrow_forwardDraw the products of the reaction shown below. Use wedge and dash bonds to indicate stereochemistry. Ignore inorganic byproducts. OSO4 (cat) (CH3)3COOH Select to Draw ઘarrow_forwardCalculate the reaction rate for selenious acid, H2SeO3, if 0.1150 M I-1 decreases to 0.0770 M in 12.0 minutes. H2SeO3(aq) + 6I-1(aq) + 4H+1(aq) ⟶ Se(s) + 2I3-1(aq) + 3H2O(l)arrow_forward
- Problem 5-31 Which of the following objects are chiral? (a) A basketball (d) A golf club (b) A fork (c) A wine glass (e) A spiral staircase (f) A snowflake Problem 5-32 Which of the following compounds are chiral? Draw them, and label the chirality centers. (a) 2,4-Dimethylheptane (b) 5-Ethyl-3,3-dimethylheptane (c) cis-1,4-Dichlorocyclohexane Problem 5-33 Draw chiral molecules that meet the following descriptions: (a) A chloroalkane, C5H11Cl (c) An alkene, C6H12 (b) An alcohol, C6H140 (d) An alkane, C8H18 Problem 5-36 Erythronolide B is the biological precursor of erythromycin, a broad-spectrum antibiotic. How H3C CH3 many chirality centers does erythronolide B have? OH Identify them. H3C -CH3 OH Erythronolide B H3C. H3C. OH OH CH3arrow_forwardPLEASE HELP! URGENT! PLEASE RESPOND!arrow_forward2. Propose a mechanism for this reaction. ہلی سے ملی N H (excess)arrow_forward
- Steps and explanationn please.arrow_forwardProblem 5-48 Assign R or S configurations to the chirality centers in ascorbic acid (vitamin C). OH H OH HO CH2OH Ascorbic acid O H Problem 5-49 Assign R or S stereochemistry to the chirality centers in the following Newman projections: H Cl H CH3 H3C. OH H3C (a) H H H3C (b) CH3 H Problem 5-52 Draw the meso form of each of the following molecules, and indicate the plane of symmetry in each: OH OH (a) CH3CHCH2CH2CHCH3 CH3 H3C. -OH (c) H3C CH3 (b) Problem 5-66 Assign R or S configurations to the chiral centers in cephalexin, trade-named Keflex, the most widely prescribed antibiotic in the United States. H2N H IHH S Cephalexin N. CH3 CO₂Harrow_forwardSteps and explanationn please.arrow_forward
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