General, Organic, and Biological Chemis...7th EditionH. Stephan Stoker Publisher: Cengage LearningISBN: 9781305767867
General, Organic, and Biological Chemis...
Solutions for General, Organic, and Biological Chemistry Seventh Edition
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Chapter 1 - Basic Concepts About MatterChapter 1.1 - Chemistry: The Strudy Of MatterChapter 1.2 - Physical States Of MatterChapter 1.3 - Properties Of MatterChapter 1.4 - Changes In MatterChapter 1.5 - Pure Substances And MixturesChapter 1.6 - Elements And CompoundsChapter 1.7 - Discovery And Abundance Of The ElementsChapter 1.8 - Names And Chemical Symbols Of The ElementsChapter 1.9 - Atoms And Molecules
Chapter 1.10 - Chemical FormulasChapter 2 - Measurements In ChemistryChapter 2.1 - Measurement SystemsChapter 2.2 - Metric System UnitsChapter 2.3 - Exact And Inexact NumbersChapter 2.4 - Uncertainty In Measurement And Significant FiguresChapter 2.5 - Significant Figures And Mathematical OperationsChapter 2.6 - Scientific NotationChapter 2.7 - Conversion FactorsChapter 2.8 - Dimensional AnalysisChapter 2.9 - DensityChapter 2.10 - Temperature ScalesChapter 3 - Atomic Structures And The Periodic TableChapter 3.1 - Internal Structure Of An AtomChapter 3.2 - Atomic Number And Mass NumberChapter 3.3 - Isotopes And Atomic MassesChapter 3.4 - The Periodic Law And The Periodic TableChapter 3.5 - Metals And NonmetalsChapter 3.6 - Electron Arrangements Within AtomsChapter 3.7 - Electronic Configurations And Orbital DiagramsChapter 3.8 - The Electronic Basis For The Periodic Law And The Periodic TableChapter 3.9 - Classification Of The ElementsChapter 4 - Chemical Bonding: The Ionic Bond ModelChapter 4.1 - Chemical BondsChapter 4.2 - Valence Electrons And Lewis SymbolsChapter 4.3 - The Octet RuleChapter 4.4 - The Ionic Bond ModelChapter 4.5 - The Sign And Magnitude Of Ionic ChargeChapter 4.6 - Lewis Structures For Ionic CompoundsChapter 4.7 - Chemical Formulas Fir Ionic CompoundsChapter 4.8 - The Structure Of Ionic CompoundsChapter 4.9 - Recognizing And Naming Binary Ionic CompoundsChapter 4.10 - Polyatomic IonsChapter 4.11 - Chemical Formulas And Names For Ionic Compounds Containing Polyatomic IonsChapter 5 - Chemical Bonding: The Covalent Bond ModelChapter 5.1 - The Covalent Bond ModelChapter 5.2 - Lewis Structures For Molecular CompoundsChapter 5.3 - Singel, Double, And Triple Covalent CompoundsChapter 5.4 - Valence Electrons And Number Of Covalent Bonds FormedChapter 5.5 - Coordinate Covalent BondsChapter 5.6 - Systematic Prodedures For Drawing Lewis StructuresChapter 5.7 - Bonding In Compounds With Polyatomic Ions PresentChapter 5.8 - Molecular GeometryChapter 5.9 - ElectronegativityChapter 5.10 - Bond PolarityChapter 5.11 - Molecular PolarityChapter 5.12 - Recognizing And Naming Binary Molecular CompoundsChapter 6 - Chemical Calculations: Formula Masses, Moles, And Chemical EquationsChapter 6.1 - Formula MassesChapter 6.2 - The Mole: A Counting Unit For ChemistsChapter 6.3 - The Mass Of A MoleChapter 6.4 - Chemical Formulas And The Mole ConceptChapter 6.5 - The Mole And Chemical CalculationsChapter 6.6 - Writing And Balancing Chemical EquationsChapter 6.7 - Chemical Equations And The Mole ConceptChapter 6.8 - Chemical Calculations Using Chemical EquationsChapter 6.9 - Yields: Theoretical, Actual, And PercentChapter 7 - Gases, Liquids, And SolidsChapter 7.1 - The Kinetic Molecular Theory Of MatterChapter 7.2 - Kinetic Molecular Theory And Physical StatesChapter 7.3 - Gas Law VariablesChapter 7.4 - Boyle's Law: A Pressure-volume RelationshipChapter 7.5 - Charle's Law: A Temperature-volume RelationshipChapter 7.6 - The Combined Gas LawChapter 7.7 - The Ideal Gas LawChapter 7.8 - Dalton's Law Of Partial PressuresChapter 7.9 - Changes Of StateChapter 7.10 - Evaporation Of LiquidsChapter 7.11 - Vapor Pressure Of LiquidsChapter 7.12 - Boiling And Boiling PointsChapter 7.13 - Intermolecular Forces In LiquidsChapter 8 - SolutionsChapter 8.1 - Characteristic Of SolutionsChapter 8.2 - SolubilityChapter 8.3 - Solution FormationChapter 8.4 - Solubility RulesChapter 8.5 - Percent Concentration UnitsChapter 8.6 - Molarity Concentration UnitChapter 8.7 - DilutionChapter 8.8 - Colloidal Dispersions And SuspensionsChapter 8.9 - Colligative Properties Of SolutionsChapter 8.10 - Osmosis And Osmotic PressureChapter 9 - Chemical ReactionsChapter 9.1 - Types Of Chemical ReactionsChapter 9.2 - Redox And Nonredox Chemical ReactionsChapter 9.3 - Terminology Associated With Redox ProcessesChapter 9.4 - Collision Theory And Chemical ReactionsChapter 9.5 - Exothermic And Endothermic Chemical ReactionsChapter 9.6 - Factors That Influence Chemical Reaction RatesChapter 9.7 - Chemical EquilibriumChapter 9.8 - Equilibrium ConstantsChapter 9.9 - Altering Equilibrium Conditions: Le Chatelier's PrincipleChapter 10 - Acids, Bases, And SaltsChapter 10.1 - Arrhenium Acid-base TheoryChapter 10.2 - Bronsted-lowry Acid-base TheoryChapter 10.3 - Mono-, Di-, And Triprotic AcidsChapter 10.4 - Strengths Of Acids And BasesChapter 10.5 - Ionization Constants For Acids And BasesChapter 10.6 - SaltsChapter 10.7 - Acid-base Neutralization Chemical ReactionsChapter 10.8 - Self-ionization Of WaterChapter 10.9 - The Ph ConceptChapter 10.10 - The Pka Method For Expressing Acid StrengthChapter 10.11 - The Ph Of Aqueous Salt SolutionsChapter 10.12 - BuffersChapter 10.13 - The Henderson-hasselbalch EquationChapter 10.14 - ElectrolytesChapter 10.15 - Equivalents And Milliequivalents Of ElectrolytesChapter 10.16 - Acid-base TitrationsChapter 11 - Nuclear ChemistryChapter 11.1 - Stable And Unstable NuclidesChapter 11.2 - The Nature Of Radioactive EmissionsChapter 11.3 - Equations For Radioactive DecayChapter 11.4 - Rate Of Radioactive DecayChapter 11.5 - Transmutation And Bombardment ReactionsChapter 11.6 - Radioactive Decay SeriesChapter 11.7 - Detection Of RadiationChapter 11.8 - Chemical Effects Of RadiationChapter 11.9 - Biochemical Effects Of RadiationChapter 11.10 - Sources Of Radiation ExposureChapter 11.11 - Nuclear MedicineChapter 11.12 - Nuclear Fission And Nuclear FusionChapter 11.13 - Nuclear And Chemical Reactions ComparedChapter 12 - Saturated HydrocarbonsChapter 12.1 - Organic And Inorganic CompoundsChapter 12.2 - Bonding Characteristics Of The Carbon AtomChapter 12.3 - Hydrocarbons And Hydrocarbon DerivativesChapter 12.4 - Alkanes: Acyclic Saturated HydrocarbonsChapter 12.5 - Structural FormulasChapter 12.6 - Alkane IsomerismChapter 12.7 - Conformation Of AlkanesChapter 12.8 - Iupac Nomenclature Of AlkanesChapter 12.9 - Line-angle Structural Fomrulas Of AlkanesChapter 12.10 - Classification Of Carbon AtomsChapter 12.11 - Branched-chain Alkyl GroupsChapter 12.12 - CycloalkanesChapter 12.13 - Iupac Nomenclature Of CycloalkanesChapter 12.14 - Isomerism In CycloalkanesChapter 12.15 - Sources Of Alkanes And CycloalkanesChapter 12.16 - Physical Properties Of Alkanes And CycloalkanesChapter 12.17 - Chemical Properties Of Alkanes And CycloalkanesChapter 12.18 - Halogenated Alkanes And CycloalkanesChapter 13 - Unsaturated HydrocarbonsChapter 13.1 - Unsaturated HydrocarbonsChapter 13.2 - Characteristics Of Alkenes And CycloalkenesChapter 13.3 - Nomenclature For Alkenes And CycloalkenesChapter 13.4 - Line-angle Structural Fomrulas Of AlkenesChapter 13.5 - Constitutional Isomerism In AlkenesChapter 13.6 - Cis-trans Isomerism In AlkenesChapter 13.7 - Naturally Occuring AlkenesChapter 13.8 - Physical Properties Of Alkenes And CycloalkenesChapter 13.9 - Preparation Of AlkenesChapter 13.10 - Chemical Reactions Of AlkenesChapter 13.11 - Polymerization Of Alkenes: Addition PolymersChapter 13.12 - AlkynesChapter 13.13 - Aromatic HydrocarbonsChapter 13.14 - Nomenclature For Aromatic HydrocarbonsChapter 13.15 - Properties Of And Sources For Aromatic HydrocarbonsChapter 13.16 - Fused-ring Aromatic HydrocarbonsChapter 14 - Alcohols, Phenols And EthersChapter 14.1 - Bonding Characteristics Of Oxygen Atoms In Organic CompoundsChapter 14.2 - Structural Characteristics Of AlcoholsChapter 14.3 - Nomenclature Of AlcoholsChapter 14.4 - Isomerism For AlcoholsChapter 14.5 - Important Commonly Encountered AlcoholsChapter 14.6 - Physical Properties Of AlcoholsChapter 14.7 - Preparation Of AlcoholsChapter 14.8 - Classification Of AlcoholsChapter 14.9 - Chemical Reactions Of AlcoholsChapter 14.10 - Structural Characteristics Of PhenolsChapter 14.11 - Nomenclature For PhenolsChapter 14.12 - Physical And Chemical Properties Of PhenolsChapter 14.13 - Occurrence Of And Use For PhenolsChapter 14.14 - Structural Characteristics Of EthersChapter 14.15 - Nomenclature For EthersChapter 14.16 - Occurrence Of And Use For EthersChapter 14.17 - Isomerism For EthersChapter 14.18 - Physical And Chemical Properties Of EthersChapter 14.19 - Cyclic EthersChapter 14.20 - Thiols: Sulfur Analogs Of AlcoholsChapter 14.21 - Thioethers: Sulfur Analogs Of EthersChapter 15 - Aldehydes And KetonesChapter 15.1 - The Carbonyl GroupChapter 15.2 - Compounds Containing A Carbonyl GroupChapter 15.3 - The Aldehyde And Ketone Functional GroupsChapter 15.4 - Nomenclature For AldehydesChapter 15.5 - Nomenclature For KetonesChapter 15.6 - Isomerism For Aldehydes And KetonesChapter 15.7 - Selected Common Aldehydes And KetonesChapter 15.8 - Physical Properties Of Aldehydes And KetonesChapter 15.9 - Preparation Of Aldehydes And KetonesChapter 15.10 - Oxidation And Reduction Of Aldehydes And KetonesChapter 15.11 - Reaction Of Aldehydes And Ketones With AlcoholsChapter 15.12 - Sulfur-containing Carbonyl GroupsChapter 16 - Carboxylic Acids, Esters, And Other Acid DerivativesChapter 16.1 - Structure Of Carboxylic Acids And Their DerivativesChapter 16.2 - Iupac Nomenclature Of Carboxylic AcidsChapter 16.3 - Common Names For Carboxylic AcidsChapter 16.4 - Polyfunctional Carboxylic AcidsChapter 16.5 - Physical Properties Of Carboxylic AcidsChapter 16.6 - Preparation Of Carboxylic AcidsChapter 16.7 - Acidity Of Carboxylic AcidsChapter 16.8 - Carboxylic Acids SaltsChapter 16.9 - Carboxylic Acid Decarboxylation ReactionsChapter 16.10 - Structures Of EstersChapter 16.11 - Preparation Of EstersChapter 16.12 - Nomenclature For EstersChapter 16.13 - Selected Common EstersChapter 16.14 - Isomerism For Carboxylic Acids And EstersChapter 16.15 - Physical Properties Of EstersChapter 16.16 - Chemical Properties Of EstersChapter 16.17 - Sulfur Analogs Of EstersChapter 16.18 - PolyestersChapter 16.19 - Acid Chlorides And Acid AnhydridesChapter 16.20 - Esters And Anhydrides Of Inorganic AcidsChapter 17 - Amines And AmidesChapter 17.1 - Bonding Characteristics Of Nitrogen Atoms In Organic CompoundsChapter 17.2 - Structura And Classification Of AminesChapter 17.3 - Nomenclature For AminesChapter 17.4 - Isomerism For AminesChapter 17.5 - Physcial Properties Of AminesChapter 17.6 - Basicity Of AminesChapter 17.7 - Reaction Of Amines With AcidsChapter 17.8 - Alkylation Of Ammonia And AminesChapter 17.9 - Heterocyclic AminesChapter 17.10 - Selected Biochemically Important AminesChapter 17.11 - AlkaloidsChapter 17.12 - Structure And Classification Of AmidesChapter 17.13 - Nomenclature Of AmidesChapter 17.14 - Selected Amides And Their UsesChapter 17.15 - Basicity Of AmidesChapter 17.16 - Physcial Properties Of AmidesChapter 17.17 - Preparation Of AmidesChapter 17.18 - Hydrolysis Of AmidesChapter 17.19 - Polyamides And PolyurethanesChapter 18 - CarbohydratesChapter 18.1 - Biochemistry-an OverviewChapter 18.2 - Occurrence And Functions Of CarbohydratesChapter 18.3 - Classification Of CarbohydratesChapter 18.4 - Chirality: Handedness In MoleculesChapter 18.5 - Stereoisomerism: Enantiomers And DiastereomersChapter 18.6 - Designating Handedness Using Fischer Projection FormulasChapter 18.7 - Properties Of EnantiomersChapter 18.8 - Classification Of MonosaccharidesChapter 18.9 - Biochemically Important MonosaccharidesChapter 18.10 - Cyclic Forms Of MonosaccharidesChapter 18.11 - Haworth Projection FormulasChapter 18.12 - Reactions Of MonosaccharidesChapter 18.13 - DisaccharidesChapter 18.14 - OligosaccharidesChapter 18.15 - General Characteristics Of PolysaccharidesChapter 18.16 - Storage PolysaccharidesChapter 18.17 - Structural PolysaccharidesChapter 18.18 - Acidic PolysaccharidesChapter 18.19 - Dietary Considerations And CarbohydratesChapter 18.20 - Glycolipids And Glycoproteins: Cell RecognitionChapter 19 - LipidsChapter 19.1 - Structure And Classification Of LipidsChapter 19.2 - Types Of Fatty AcidsChapter 19.3 - Physical Properties Of Fatty AcidsChapter 19.4 - Energy-storage Lipids: TriacylglycerolsChapter 19.5 - Dietary Considerations And TriacylglycerolsChapter 19.6 - Chemical Reactions Of TriacylglycerolsChapter 19.7 - Membrane Lipids: PhospholipidsChapter 19.8 - Membrane Lipids: SphingoglycolipidsChapter 19.9 - Membrane Lipids: CholesterolChapter 19.10 - Cell MembranesChapter 19.11 - Emulsification Lipids: Bile AcidsChapter 19.12 - Messenger Lipids: Steroid HormonesChapter 19.13 - Messenger Lipids: EicosanoidsChapter 19.14 - Protective-coating Lipids: Biological WaxesChapter 19.15 - Saponifiable And Nonsaponifiable LipidsChapter 20 - ProteinsChapter 20.1 - Characteristics Of ProteinsChapter 20.2 - Amino Acids: The Building Blocks For ProteinsChapter 20.3 - Essential Amino AcidsChapter 20.4 - Chirality And Amino AcidsChapter 20.5 - Acid-base Properties Of Amino AcidChapter 20.6 - Cysteine: A Chemically Unique Amino AcidChapter 20.7 - PeptidesChapter 20.8 - Biochemically Important Small PeptidesChapter 20.9 - General Structural Characteristics Of ProteinsChapter 20.10 - Primary Structure Of ProteinsChapter 20.11 - Secondary Structure Of ProteinsChapter 20.12 - Tertiary Structure Of ProteinsChapter 20.13 - Quaternary Structure Of ProteinsChapter 20.14 - Protein HydrolysisChapter 20.15 - Protein DenaturationChapter 20.16 - Protein Classification Based On ShapeChapter 20.17 - Protein Classification Based On FunctionChapter 20.18 - GlycoproteinsChapter 20.19 - LipoproteinsChapter 21 - Enzymes And VitaminsChapter 21.1 - General Characteristics Of EnzymeChapter 21.2 - Enzyme StructureChapter 21.3 - Nomenclature And Classification Of EnzymesChapter 21.4 - Models Of Enzyme ActionChapter 21.5 - Enzyme SpecificityChapter 21.6 - Factors That Affect Enzyme ActivityChapter 21.7 - ExtremozymesChapter 21.8 - Enzyme InhibitionChapter 21.9 - Regulation Of Enzyme ActivityChapter 21.10 - Prescription Drugs That Inhibit Enzyme ActivityChapter 21.11 - Medical Uses Of EnzymesChapter 21.12 - General Characteristics Of VitaminsChapter 21.13 - Water-soluble Vitamins: Vitamin CChapter 21.14 - Water-soluble Vitamins: The B VitaminsChapter 21.15 - Fat-soluble VitaminsChapter 22 - Nucleic AcidsChapter 22.1 - Types Of Nucleic AcidsChapter 22.2 - Nucleotides: Structural Building Blocks For Nucleic AcidsChapter 22.3 - Nucleotide FormationChapter 22.4 - Primary Nucleic Acid StructureChapter 22.5 - The Dna Double HelixChapter 22.6 - Replication Of Dna MoleculesChapter 22.7 - Overview Of Protein SynthesisChapter 22.8 - Ribonucleic AcidsChapter 22.9 - Transcription: Rna SynthesisChapter 22.10 - The Genetic CodeChapter 22.11 - Anticodons And Trna MoleculesChapter 22.12 - Translatio: Protein SynthesisChapter 22.13 - MutationsChapter 22.14 - Nucleic Acids And VirusesChapter 22.15 - Recombinant Dna And Genetic EngineeringChapter 22.16 - The Polymerase Chain ReactionChapter 23 - Biochemical Energy ProductionChapter 23.1 - MetabolismChapter 23.2 - Metabolism And Cell StructureChapter 23.3 - Important Nucleotide-containing Compounds In Metabolic PathwaysChapter 23.4 - Important Carboxylate Ions In Metabolic PathwaysChapter 23.5 - High-energy Phosphate CompoundsChapter 23.6 - An Overview Of Biochemical Energy ProductionChapter 23.7 - The Citric Acid CycleChapter 23.8 - The Electron Transport ChainChapter 23.9 - Oxidative PhosphorylationChapter 23.10 - Atp Production For The Common Metabolic PathwayChapter 23.11 - Non-etc Oxygen-consuming ReactionsChapter 23.12 - B Vitamins And The Common Metabolic PathwayChapter 24 - Carbohydrate MetabolismChapter 24.1 - Digestion And Absorption Of CarbohydratesChapter 24.2 - GlycolysisChapter 24.3 - Fates Of PyruvateChapter 24.4 - Atp Production From The Complete Oxidation Of GlucoseChapter 24.5 - Glycogen Synthesis And DegradationChapter 24.6 - GluconeogenesisChapter 24.7 - Terminology For Glucose Metabolic PathwaysChapter 24.8 - The Pentose Phosphate PathwayChapter 24.9 - Hormonal Control Of Carbohydrate MetabolismChapter 24.10 - B Vitamins And Carbohydrate MetabolismChapter 25 - Lipid MetabolismChapter 25.1 - Digestion And Absorption Of LipidsChapter 25.2 - Triacylglycerol Storage And MobilizationChapter 25.3 - Glycerol MetabolismChapter 25.4 - Oxidation Of Fatty AcidsChapter 25.5 - Atp Production From Fatty Acid OxidationChapter 25.6 - Ketone Bodies And KetogenesisChapter 25.7 - Biosynthesis Of Fatty Acids: LipogenesisChapter 25.8 - Relationships Between Lipogenesis And Citric Acid Cycle IntermediatesChapter 25.9 - Fate Of Fatty-acid-generated Acetyl CoaChapter 25.10 - Relationships Between Lipid And Carbohydrate MetabolismChapter 25.11 - B Vitamins And Lipid MetabolismChapter 26 - Protein MetabolismChapter 26.1 - Protein Digestion And AbsorptionChapter 26.2 - Amino Acid UtilizationChapter 26.3 - Transamination And Oxidative DeaminationChapter 26.4 - The Urea CycleChapter 26.5 - Amino Acid Carbon SkeletonsChapter 26.6 - Amino Acid BiosynthesisChapter 26.7 - Hemoglobin CatabolismChapter 26.8 - Proteins And The Element SylfurChapter 26.9 - Interrelationships Among Metabolic PathwaysChapter 26.10 - B Vitamins And Protein Metabolism
Book Details
Emphasizing the applications of chemistry and minimizing complicated mathematics, GENERAL, ORGANIC, AND BIOLOGICAL CHEMISTRY, 7E is written throughout to help students succeed in the course and master the biochemistry content so important to their future careers. The Seventh Edition's clear explanations, visual support, and effective pedagogy combine to make the text ideal for allied health majors. Early chapters focus on fundamental chemical principles while later chapters build on the foundations of these principles. Mathematics is introduced at point-of-use and only as needed.
Sample Solutions for this Textbook
We offer sample solutions for General, Organic, and Biological Chemistry Seventh Edition homework problems. See examples below:
Chapter 1, Problem 1.1EPGiven chemical notation is Li2CO3. As there are more than one element present in the given chemical...Given chemical notation is Hf. As there are only one atom present in the given chemical notation, it...Given chemical formulas are HN3 and NH3. Total number of atoms in HN3: This contains one hydrogen...Given chemical formulas are NO2 and N2O. Total number of atoms in NO2: This contains one nitrogen...Chapter 1, Problem 1.85EPChapter 1, Problem 1.86EPGiven molecules in mixture are N2, N2H4, NH3, CH4, and CH3Cl. Number of atoms in N2: As this...Chapter 1, Problem 1.88EP
Chapter 2, Problem 2.1EPChapter 2, Problem 2.33EPChapter 2, Problem 2.34EPThe number of significant figures in the answer after solving a multiplication or division problem...Chapter 2, Problem 2.50EPChapter 2, Problem 2.51EPChapter 2, Problem 2.52EPGiven scientific notation is (3.20 x 107) x (1.720 x 105). The coefficient has to be multiplied and...Given scientific notation is (4.0 x 104) x (1.32 x 108). The coefficient has to be multiplied and...Density can be calculated using the below formula. Density = (massvolume) 1.0 g and 2.0 cm3 are the...Chapter 2, Problem 2.100EPChapter 3, Problem 3.1EPChapter 3, Problem 3.5EPGiven atom is said to have atomic number as 8 and mass number as 18. The number of protons,...Given atom is S50118n. From this it is understood that the atomic number is 50 and mass number is...Given atom is F2658e. From this it is understood that the atomic number is 26 and mass number is 58....Chapter 3, Problem 3.21EPChapter 3, Problem 3.22EPGiven chemical symbol is N1123a. The total number of subatomic particles in any atom is the sum of...Chapter 3, Problem 3.24EPFor N713: The atomic number is given as 7. The element is found to be nitrogen. Mass number given...For A1840r: The atomic number is given as 18. The element is found to be argon. Mass number given...Chapter 3, Problem 3.78EPChapter 4, Problem 4.1EPChapter 4, Problem 4.28EPChapter 4, Problem 4.29EPChapter 4, Problem 4.30EPCa2+ ion combines with F- ions combine in 1 to 2 ratio because this combination causes the resultant...Br- ion combines with Na+ ions combine in 1 to 1 ratio because this combination causes the resultant...Chapter 4, Problem 4.68EPThe given two ions are Al3+ and CN-. Three cyanide ions (1- charge) are required to balance the...The given two ions are Cu2+ and OH-. Two hydroxide ions (1- charge) are required to balance the...The given name of the compound has Al3+ and CO32- ions. Aluminium ion has +3 charge and carbonate...The given name of the compound has Ca2+ and PO43- ions. Calcium ion has +2 charge and phosphate ion...The given name of the compound has BaBr2 chemical formula. The dissociation of BaBr2 is as follows:...The given name of the compound has Cu2SO4 chemical formula. The dissociation of Cu2SO4 is as...Chapter 5, Problem 5.1EPGiven triatomic molecule is, The central atom in the above molecule is found to be sulfur. This has...Given triatomic molecule is, The central atom in the above molecule is found to be carbon. This has...Given molecule is, The central atom in the above molecule is found to be nitrogen. This has three...Chapter 5, Problem 5.55EPGiven molecule is SiH4. The Lewis structure for SiH4 can be drawn as shown below, The above drawn...Chapter 5, Problem 5.58EPChapter 5, Problem 5.87EPChapter 5, Problem 5.88EPGiven compounds are N2O3, KCl, HF, CH4, and CO2. For N2O3: This contains nitrogen and oxygen as its...Given compounds are NH3, Na2O, H2S, N2H4, and CO. For NH3: The elements present in the given...Chapter 6, Problem 6.1EPChapter 6, Problem 6.43EPChapter 6, Problem 6.47EPChapter 6, Problem 6.48EPGiven chemical equation is Na + H2O → NaOH + H2. Looking into the equation, the element that is...Chapter 6, Problem 6.50EPGiven chemical equation is CH4 + O2 → CO2 + H2O. Looking into the equation, it is found that the...Chapter 6, Problem 6.52EPChapter 6, Problem 6.63EPChapter 7, Problem 7.1EP(a) Record the given data, V1 = ?T1 = 100°C converted to 373K V2 = 1.0LT2 = 110°C converted to 383K...(a) Record the given data, V1 = 3.30LT1 = 165°C converted to 438K V2 = ?T2 = 265°C converted to 538K...Record the given data, P1=1.35 atmV1 = 15.2 LT1 = 33°C converted to 306KP2 = 3.50 atmT2 = 35°C...Record the given data, P1=735 mm HgV1 = 7.31 LT1 = 45°C converted to 318KP2 = ?T2 = 357°C converted...(a) Record the given data, P = ?V =2.00 Ln = 2.00 moleT = 127°C converted to 400K Now, substitute...(a) Record the given data, P = 22.4 atmV = ?n = 3.00 moleT = 27°C converted to 300K Now, substitute...Chapter 7, Problem 7.51EPChapter 7, Problem 7.52EPRecord the given data, P = ?V = 4.00Ln = 0.72 moleT = 40°C converted to 313KR = 0.821 atm.L/mole.K...Record the given data, P = ?V = 2.00Ln = 0.50 moleT = 50°C converted to 323KR = 0.821 atm.L/mole.K...Reason for true statements: Option a): In a solution, more than one substance can dissolve in a...Given information: Initial volume of solution = 25.0 mL Initial concentration = 0.220 M Final volume...Given information: Initial volume of solution = 35.0 mL Initial concentration = 1.25 M Final volume...Given information: Volume of solution = 50.0 mL Initial concentration = 3.00 M Required...Given information: Volume of solution = 25.0 mL Initial concentration = 1.00 M Required...Given information: Initial volume of solution = 30.0 mL Initial concentration = 5.0 M Final volume...Given information: Initial volume of solution = 20.0 mL Initial concentration = 5.0 M Final volume...Given that 1.0 mol of sucrose is added to make a solution in 0.25 kg of water. The addition of one...Chapter 8, Problem 8.95EPChapter 8, Problem 8.96EPChapter 8, Problem 8.99EPGiven data is as follows: KNO3 = 1 M Osmolarity can be determined by the equation given below:...Chapter 9, Problem 9.1EPChapter 9, Problem 9.9EPChapter 9, Problem 9.71EPChapter 9, Problem 9.72EPChapter 9, Problem 9.73EPThe given reaction is: 2SO2(g) + O2(g) ⇌ 2SO3(g) The equilibrium constant, Keq=[SO3]2[SO2]2[O2]The given reaction is: H2(g) + Br2(g) ⇌ 2HBr(g) Given, Keq(25oC) = 2.0×109 The value of Keq is very...Chapter 9, Problem 9.78EPThe given reaction is: C6H6(g) + 3H2(g) ⇌ C6H12(g) + heat On increasing the concentration of C6H12...Chapter 9, Problem 9.90EPChapter 10, Problem 10.1EPGiven, Hydroxide ion concentration = 3.5×10-3 MIon product constant for water = 1.0×10−14 M To...Chapter 10, Problem 10.66EPChapter 10, Problem 10.67EPGiven, Hydroxide ion concentration = 4.2×10-4 MIon product constant for water = 1.0×10−14 M To...Given, Hydronium ion concentration = 5.5×10-2 MIon product constant for water = 1.0×10−14 M To...Given, Hydronium ion concentration = 2.4×10-3 MIon product constant for water = 1.0×10−14 M To...Given, Hydronium ion concentration = 5.5×10-2 MIon product constant for water = 1.0×10−14 M To...Chapter 10, Problem 10.72EPChapter 10, Problem 10.85EPGiven that, [OH-] = 7.2×10−5 Then, Kw = [H+] [OH-][H3O+] [OH-] = 1×10-14[H3O+] =...According to definition of pH, pH = −log[H3O+] Hence for 1.0 M HCl, pH = −log[H3O+]pH = −log 1.0pH =...Given data is shown below: Concentration of Na+ = 75 mEqConcentration of K+ = 25 mEqConcentration of...Given data is shown below: Concentration of Na+ = 75 mEqConcentration of K+ = 25 mEqConcentration of...Chapter 10, Problem 10.149EPChapter 10, Problem 10.150EPGiven nuclide is B410e. In this the number 10 present in the superscript is the mass number (number...Given decay reaction is polonium-210 to lead-206. The atomic number of polonium is 82. Atomic number...Given decay reaction is potassium-40 to calcium-40. The atomic number of potassium is 19. Atomic...Given nuclear reaction is beta emission produces mercury-199 as product. This can be represented as,...Given nuclear reaction is beta emission produces thallium-206 as product. This can be represented...Half-life of the radionuclide is given as 6.0 hr. The number of half-lives can be calculated as...Half-life of the radionuclide is given as 5.0 min. The number of half-lives can be calculated as...Number of half-lives can be determined as shown below, (12n) = 116(12n) = 1242n = 24 As the bases...Number of half-lives can be determined as shown below, (12n) = 18(12n) = 1232n = 23 As the bases are...Given description is an alpha particle bombards with beryllium-9 to give a neutron product. The...Given statement states that the total number of organic compounds exceeds the number of inorganic...Alkanes are saturated hydrocarbons that contain only single bonds between carbon atoms with no ring...Alkanes are saturated hydrocarbons that contain only single bonds between carbon atoms with no ring...Cycloalkanes are saturated hydrocarbons that contain only single bonds between carbon atoms with a...Chapter 12, Problem 12.94EPGiven cycloalkane is, The above structure is a line-angle structural formula representation. This...Given cycloalkane is, The above structure is a line-angle structural formula representation. This...Given name of cycloalkane is 1,2-dimethylcyclohexane. From the name it is understood that the parent...Given name of cycloalkane is 1,2-dimethylcyclopentane. From the name it is understood that the...Halogenation is a chemical reaction between a substance and halogen. The product of halogenation...Chapter 12, Problem 12.134EPCycloalkanes are saturated hydrocarbons that contain only single bonds between carbon atoms with a...Cycloalkanes are saturated hydrocarbons that contain only single bonds between carbon atoms with a...The alkane chemical formula given is CH3Cl. On chlorination of methane, four products can be...The alkane chemical formula given is CHCl3. On chlorination of methane, four products can be...Chapter 13, Problem 13.1EPAlkenes are one of the types of unsaturated hydrocarbon. Alkenes contain double bond as the...Chapter 13, Problem 13.10EPGiven molecular formula is C6H12. Considering the general molecular formula for alkene, the value of...Given molecular formula is C4H8. Considering the general molecular formula the value of “n” is 4....Cyclolkanes are saturated hydrocarbons that contain only single bonds between carbon atoms with ring...Chapter 13, Problem 13.28EPGiven structure is, Carbon atoms are present at the intersection and at the end points. The above...Given structure is, Carbon atoms are present at the intersection and at the end points. The above...Given structure is, Looking into the left most carbon atom present in the given structure, it is not...Given structure is, Looking into the left most carbon atom present in the given structure, it is not...Given compound is, The longest continuous carbon chain present in the given compound is five carbon...Given compound is, The longest continuous carbon chain present in the given compound is two carbon...Chapter 13, Problem 13.110EPOxygen is a Group VIA element. Therefore, it has six valence electrons. All the elements try to...Given name of alcohol is pentyl alcohol. From the name it is identified that the alkyl group is...Given name of alcohol is butyl alcohol. From the name it is identified that the alkyl group is butyl...Chapter 14, Problem 14.19EPGiven name of alcohol is 3-ethyl-2-butanol. From the name it is identified that the parent alkane is...Given structure of alcohol is, The longest carbon chain in the above structure with the hydroxyl...Given structure of alcohol is, The longest carbon chain in the above structure with the hydroxyl...In organic chemistry, oxidation reaction is said to be decrease in C−H bonds or increase in C−O...In organic chemistry, oxidation reaction is said to be decrease in C−H bonds or increase in C−O...The structure of given compound is shown below, First step is to identify the longest carbon chain....The structure of given compound is shown below, First step is to identify the longest carbon chain....Chapter 14, Problem 14.139EPGiven structure of compound is shown below, First step is to identify the longest continuous carbon...Given structure of compound is shown below, First step is to identify the longest carbon chain. In...Given structure of compound is shown below, First step is to identify the longest carbon chain. In...Given compound is, In the above structure, a double bond is present between the carbon and oxygen...The given name of the compound is 3-methylpentanal. From the name it is understood that the parent...The given name of the compound is 2-methylpentanal. From the name it is understood that the parent...The given name of the compound is formaldehyde. From the name it is understood that the parent...The given name of the compound is 3-methyl-2-pentanone. From the name it is understood that the...The given name of the compound is 2-methyl-3-pentanone. From the name it is understood that the...The given name of the compound is 2-butanol. From the name it is understood that the parent carbon...The given name of the compound is propanal. From the name it is understood that the parent carbon...Aldehydes undergo Tollen’s test. The product formed when aldehyde undergo oxidation is a carboxylic...Aldehydes undergo Tollen’s test. The product formed when aldehyde undergo oxidation is a carboxylic...Aldehydes undergo Tollen’s test. The product formed when aldehyde undergo oxidation is a carboxylic...Chapter 15, Problem 15.80EPReason for correct option: Carboxylic acid is a class of organic compound that contain carbonyl...The general structure of carboxylic acid derivatives is, The atom in entity Z that is bonded to the...The general structure of carboxylic acid is, The atom in entity Z that is bonded to the carbonyl...Given structure of carboxylic acid is, The longest continuous carbon chain has to be found out with...Given name of carboxylic acid is 2,2-dimethylbutanoic acid. From the name it is identified that the...Given name of carboxylic acid is 2,3-dichlorohexanoic acid. From the name it is identified that the...Given description about the carboxylic acid is α-chlorobutyric acid. In the problem statement it is...Given description about the carboxylic acid is chloroacetic acid. In the problem statement it is...Structure of acrylic acid is, The longest continuous carbon chain has to be found out with the...Structure of fumaric acid is, The longest continuous carbon chain has to be found out with the...Primary alcohol on oxidation gives aldehyde as intermediate product. This on further oxidation gives...Aldehyde on oxidation gives carboxylic acid as the product. The general scheme can be represented as...Given carboxylic acid salt is sodium butanoate. The structure of sodium butanoate can be given as...Given carboxylic acid salt is calcium propanoate. The structure of calcium propanoate can be given...Given carboxylic acid and alcohol structure is, The reaction between two compounds that are shown...Given carboxylic acid and alcohol structure is, The reaction between two compounds that are shown...Given name of ester is ethyl pentanoate. The structure of ethyl pentanoate can be given as, Under...Carbon is an element that belongs to group IVA in periodic table. This means the valence electrons...Given amine salt is CH3−CH2−CH2−N+H3 Cl−. The parent amine can be found by deprotonating the amine...Given amine salt is, The parent amine can be found by deprotonating the amine salt. This can be...Given reaction is, The reactants given in the above reaction are ammonia, propyl chloride. Sodium...Given reaction is, The reactants given in the above reaction are ammonia, isopropyl chloride. Sodium...Given reaction is, The reactants given in the above reaction are ammonia, propyl chloride. Sodium...Given reaction is, The reactants given in the above reaction are ammonia, isopropyl chloride. Sodium...Given reactants are trimethylamine and ethyl bromide. In this, the amine given is a tertiary amine....Given reactants are dimethylamine and propyl bromide. In this, the amine given is a secondary amine....The given name of the compound is N,N-diethylpropanamide. From the name it is understood that the...Given reaction is, In amidification process, −OH from carboxylic acid and −H from amine or ammonia...Given reaction is, In amidification process, −OH from carboxylic acid and −H from amine or ammonia...Given reaction is, In amidification process, −OH from carboxylic acid and −H from amine or ammonia...Given reaction is, In amidification process, −OH from carboxylic acid and −H from amine or ammonia...Given structure of compound is, As the nitrogen atom present in the above amide has two hydrogen...Given structure of compound is, As the nitrogen atom present in the above amide has two hydrogen...Given reaction is, The starting material is a carboxylic acid and a primary amine. The product...It is usually misconcepted that the human body contains a major part of the organic substances. The...The most of the properties of (+)−lactic acid and (−)−lactic acid are same. But the properties...The most of the properties of (+)− glyceraldehyde and (−)− glyceraldehyde are same. But the...The monosaccharide, D−glucose is an aldohexose sugar because it contains six carbon atoms attached...The given molecule is D−glucose. The molecular formula of D−glucose is C6H12O6. The Fisher...The given Haworth projection formula is shown as, Thus, in this Haworth projection formula of the...The given Haworth projection formula is shown as, Thus, in this Haworth projection formula of the...The given Haworth projection formula is shown as, The open-chain form of the given Haworth...The given Haworth projection formula is shown as, The open-chain form of the given Haworth...The given Haworth projection formula is shown as, The open-chain form of the given Haworth...The given Haworth projection formula is shown as, The open-chain form of the given Haworth...The given monosaccharide is α−D−galactose. The open-chain structure of α−D−galactose is, The Haworth...The given monosaccharide is α−D−mannose. The open-chain structure of α−D−mannose is, The Haworth...The Fisher projection formula for D-allose is, The structure given in Problem 18-103 is, The above...The Fisher projection formula for D-allose is, The structure given in Problem 18-104 is, The above...Amylopectin is a branched polysaccharide of starch. Only one type of monosaccharide, glucose is...Amylose is an unbranched polysaccharide of starch. The glycosidic linkage present in amylose is...Amylose is an unbranched polysaccharide of starch. The glycosidic linkage present in amylose is...Chapter 19, Problem 19.1EPProteins are the naturally occurring organic molecules that are composed of amino acids. Amino acids...Chapter 21, Problem 21.1EPChapter 22, Problem 22.1EPThe given DNA template strand is 5' ATAT 3'. Its corresponding informational DNA strand is 3' TATA...The given DNA template strand is 5' TAAT 3'. Its corresponding informational DNA strand is 3' ATTA...Chapter 22, Problem 22.135EPChapter 22, Problem 22.136EPChapter 22, Problem 22.137EPChapter 22, Problem 22.138EPChapter 23, Problem 23.1EPNicotinamide adenine dinucleotide exists in two forms: NADH and NAD+. The structure consists of...The structure of NAD+ consists of three subunits: nicotinamide, ribose, and ADP. ADP is a nucleotide...The structure of ATP is: The structure of FAD is: The structure of NAD+ is: Here, R=Ribose-ADP. The...Step 3 is the first step where both the oxidation and decarboxylation occurs. Step 3 involves the...In the electron transport chain, electrons are transferred from complex I and II to complex III...In the complex, I initially, NADH is oxidized and releases two electrons that reduce FMN molecule...Fe(III)SP is a structural component of the complex I and consists of iron that changes its oxidation...FMNH2 is the structural component of the complex I of the electron transport chain. Flavin...Chapter 23, Problem 23.89EPIn the complex II, electrons are transferred from the FADH2 molecule produced in the citric acid...Complex I consists of more than 40 structural subunits. Its structure has B-vitamin-containing...Complex II consists of four subunits in its structure. This complex interacts initially with the...Oxaloacetate undergoes condensation reaction in the first step of the citric acid cycle. The first...Chapter 24, Problem 24.1EPThe structure of fructose 6−phosphate is as follows: Here, denotes the PO32− unit. The intermediate...The structure of 2−Phosphoglycerate is as follows: Here, denotes the PO32− unit. The intermediate...In step 7 and step 10, two ATP molecules are produced in each step. Hence, in the glycolysis...The first step in the glycolysis process is the phosphorylation of glucose using ATP. Glucose is...Reason for correct choice: Under aerobic conditions, pyruvate is converted to acetyl CoA by the...Reason for correct choice: In the ethanol fermentation process, pyruvate is converted to ethanol and...Reason for correct option: Under aerobic conditions, pyruvate is converted to acetyl CoA by the...In the glycolysis metabolic pathway, a glucose molecule breaks down and is converted into two...An overview of the Cori cycle is as follows: Lactate is converted to pyruvate in the liver....An overview of the Cori cycle is as follows: Lactate is converted to pyruvate in the liver and...B vitamin thiamin is encountered in the form of thiamin pyrophosphate (TPP) in the carbohydrate...Chapter 25, Problem 25.1EPThe first stage of glycerol metabolism is a two-step process. In step 1, glycerol 3−phosphate is...The enzymes that are needed for the oxidation of fatty acid are located in the mitochondrial matrix....The reaction in step 1 of a turn of the β−oxidation pathway is a dehydrogenation reaction in which...In step 1 of a turn of the β−oxidation pathway, hydrogen atoms from the α and β carbons of acyl CoA...The first stage of glycerol metabolism is a two-step process. In step 1, glycerol-3-phosphate is...The first stage of glycerol metabolism is a two-step process. In step 1, glycerol-3-phosphate is...All three processes involve four distinct reactions. The four distinct reactions involved in...Enoyl CoA is a product in step 1 of the β-oxidation pathway. Step 1 is a dehydrogenation reaction....HMG-CoA is produced in step 2 in ketogenesis. Step 2 is a condensation reaction. In step 2,...Intermediates involved in the lipogenesis are derivative of C4 molecule butyric acid. Butyric acid...Succinic acid is a dicarboxylic acid and has 4 carbon atoms. Thus, each intermediate of the citric...Reason for correct option: Denaturation of proteins can be effected by treatment of protein with...Glutamate is an amino acid and its structure is: α-ketoglutarate is keto acid and its structure is:...α-ketoglutarate is keto acid and its structure is: Oxaloacetate is a keto acid and its structure is:...Glutamate is an amino acid and its structure is: Aspartate is an amino acid and its structure is:...In both transamination and oxidative deamination reaction exchange of an amino group from an α-amino...Oxaloacetate is a keto acid. In both transamination and oxidative deamination reaction exchange of...The structure of oxaloacetate is: Oxaloacetate contains both a carbonyl group and a carboxyl...Ornithine is a nonstandard amino acid and accepts the entering carbamoyl phosphate group at the...Carbamoyl phosphate and aspartate are fuel for the urea cycle. The structure of carbamoyl phosphate...Coenzyme nicotinamide adenine dinucleotide (NAD+) and nicotinamide adenine dinucleotide phosphate...Coenzyme flavin adenine dinucleotide (FAD) contains the B vitamin riboflavin in its structure....
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