Chemistry in Sickness and Health: A Survey for Allied Health Professionals

Edition: 1

Copyright: 2025

Pages: 618

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$75.00 USD

ISBN 9798385171583

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This textbook provides a comprehensive foundation in health sciences and chemistry, beginning with the essential principles of scientific measurement and progressing through the structure and behavior of matter. Early chapters introduce key topics such as significant figures, scientific notation, unit conversions, precision and accuracy, and the classification of measurement systems. The text then builds toward a deeper understanding of atomic structure, the periodic table, chemical bonding, energy and matter, and the properties of solutions and chemical reactions, establishing a strong conceptual and quantitative base for scientific study.

In its later chapters, the book transitions into a detailed exploration of organic and biochemistry, including acids and bases, hydrocarbons, functional groups, biomolecules (such as carbohydrates, lipids, proteins, and nucleic acids), and metabolic processes. It also covers enzymes, cellular energy production, and genetic principles such as DNA replication, transcription, and protein synthesis. Supporting appendices provide reference materials on periodic trends, functional groups, molecular geometry, common ions, and biochemical cycles. 

Chapter 1: The Units of Measurements in Health Sciences

  1. The Scientific Method and Precise Measurements
  2. Significant Figures: Mastering Precision in Scientific Measurements
    • Examples
  3. How to Round Numbers
  4. Calculating Results with Significant Figures
  5. Significant Figures in Addition/Subtraction and Multiplication/Division
    • Addition and Subtraction
    • Multiplication and Division
  6. Scientific Notation
    • Performing Calculations Using Scientific Notation
  7. Measured Numbers
  8. Precision and Accuracy: Cornerstones of Reliable Chemistry
    • High Precision–High Accuracy
    • High Precision–Low Accuracy
    • Low Precision–High Accuracy
    • Low Precision–Low Accuracy
  9. The Units of Measurement
  10. Conventional (British or Imperial) Units
  11. Metric Units
  12. Scientific Units (SI)
  13. Converting Units
  14. Conversion Factors from One Unit to Another
  15. Base and Derived Units
  16. Mass, Volume, and Density
  17. Temperature Scales: °C, °F, and K
  • Celsius Scale (°C)
  • Fahrenheit Scale (°F)
  • Kelvin Scale (K)
  1. Health Notes
    Key Terms

Chapter 2: Atoms, Elements, Compounds, and Mixtures

  1. Atoms, Elements, Compounds, and Mixtures
  2. Physical and Chemical Properties
  3. Types of Mixtures (Homogeneous and Heterogeneous) and Separation Techniques
  4. Organization and Structure of the Periodic Table
  5. Key Information Provided by the Periodic Table
  6. Atomic Number and Atomic Mass
  7. Element Symbols and Names
    • Uranium (U)
    • Einsteinium (Es)
    • Californium (Cf)
    • Sodium (Na)
    • Special Note
  8. Periodic Trends and Element Properties
    • Ionization Energy and Electronegativity
    • Metallic and Nonmetallic Character
    • Reactivity and Group Trends
    • Ionic Sizes
    • Electrolytes and Biochemical Processes
  9. Writing Lewis (Dot) Structures
    • Valence Electrons
  10. Atomic Number, Protons, and Electrons
  • Hydrogen Example
  • Oxygen Example
  1. Avogadro’s Number and the Mole
  2. Mole Conversions (Particles and Mass)
  • Moles to Particles
  • Particles to Moles
  • Moles to Mass
  • Mass to Moles
    Key Terms

Chapter 3: Types of Chemical Bonds

  1. Covalent Bonds and the Octet Rule
    • Covalent Bonds
    • Octet Rule
    • Examples
  2. Lewis Structures
    • Basics
    • Construction
  3. Naming Molecules
    • Rules
    • Examples
  4. Single, Double, and Triple Bonds
  5. Ionic Bonds
    • Examples
  6. Electronegativity and Polar Bonds
    • Characteristics
    • Examples
  7. Polyatomic Ions
    • Examples
  8. Ionic Compound Formulas
    • Rules
  9. Covalent vs Ionic Compounds
  10. Transition Metal Compounds
  11. Metallic Bonds
    Key Terms

Chapter 4: Energy and Matter

  1. Matter, Heat, and Energy
    • Energy and Chemical Reactions
    • Units of Energy
    • Measurement of Energy Content
  2. States of Matter (Solid, Liquid, Gas, Plasma)
  3. Changes in Physical State
    • Phase Diagrams and Cooling Curves
  4. Properties of Gases and Gas Laws
  5. Attractive Forces
  6. Solutions and Dissolving
  7. Renewable and Sustainable Energy
    Key Terms

Chapter 5: Concentrations of Solutions

  1. Solutions
  2. Electrolytes and Nonelectrolytes
  3. Solubility
  4. Factors Affecting Solubility (T, P, Polarity)
    • Temperature
    • Pressure
    • Polarity
    • Applications
    • Saturated, Unsaturated, Supersaturated Solutions
  5. Percent Concentration
  6. Molarity (M) and Molality (m)
  7. Equivalents
  8. Dilution of Solutions
  9. Osmosis and Dialysis
  10. Tonicity
  • Colligative Properties
    Key Terms

Chapter 6: Chemical Reactions

  1. Writing Chemical Equations
  2. Balancing Chemical Equations
    • Steps 1–4
  3. Molar Mass
    • Examples
  4. Mass–Mole Relations
  5. Chemical Reaction Calculations
  6. Enthalpy Changes and Energy Diagrams
    • Endothermic Reactions
  7. Reaction Rate and Catalysts
    Key Terms

Chapter 7: Acids and Bases

  1. Self-Ionization of Water
  2. Properties of Acids and Bases
    • Broader Definitions
  3. Weak Acid/Base Equilibrium Constants
  4. pH Scale
  5. Acid–Base Reactions
  6. Conjugate Acids and Bases
  7. Buffers
    • Henderson–Hasselbalch Equation
      Key Terms

Chapter 8: Introduction to Organic Chemistry

  1. Hydrocarbons
  2. Elements in Organic Molecules (C, H, O, N)
    • Carbon
    • Hydrogen
    • Oxygen
    • Nitrogen
  3. Alkanes
  4. Linear, Branched, and Cyclic Alkanes
    • Skeletal Representation
  5. Geometry of Alkanes
    • Alkyl Groups
  6. Nomenclature of Alkanes
  7. Alkenes
  8. Geometry of Alkenes
  9. Cis-Trans Isomers
  10. Aromatic Compounds
  11. Alkene Nomenclature
  12. Alkynes
  13. Geometry of Alkynes
  14. Alkynes Nomenclature
  15. Hydrocarbon Properties
  • Environmental Impact
    Key Terms

Chapter 9: Alcohols, Ethers, Thiols, and Phenols

  1. Alcohols: Structure and Characteristics
  2. Alcohol Nomenclature
    • IUPAC Rules
    • Classification
  3. Chirality
  4. Hydration of Alkenes
  5. Dehydration of Alcohols (Zaitsev’s Rule)
  6. Ether Formation (Condensation Reactions)
  7. Thiols and Phenols
  8. Physical Properties of Functional Groups
    Key Terms

Chapter 10: Carbonyl Compounds and Redox Reactions

  1. Carbonyl Compounds
  2. Aldehydes and Ketones
  3. Nomenclature and Properties
    • Aldehydes
    • Ketones
    • Physical Properties
  4. Oxidation and Reduction Reactions
    • Oxidation
    • Reduction
  5. Addition Reactions
  6. Carboxylic Acids and Esters
  7. Reactions of Carboxylic Acids
    • Emulsification, Saponification, Surfactants
  8. Physical Properties of Acids and Esters
  9. Biological Redox Reactions
  10. Thioesters and Phosphoesters in Biology
    Key Terms

Chapter 11: Amines and Amides

  1. Nitrogen in the Environment and Organic Compounds
  2. Naming Simple Amines and Amides
  3. Types of Amines
    • Physical Properties of Amines
  4. Alkaloids
  5. Amines as Bases
    • Quaternary Ammonium Salts
  6. Neurotransmitters
  7. Vitamins
  8. Amino Acids
  9. Amides
  10. Hydrolysis of Amides
  11. Nitrogen-Containing Plastics and Polymers
    Key Terms

Chapter 12: Amino Acids, Proteins, and Enzymes

  1. General Structure of Amino Acids
  2. Acid-Base Characteristics of Amino Acids
  3. Essential Amino Acids
  4. Proteins
  5. Protein Structure (Primary, Secondary, Tertiary, Quaternary)
    • Primary Structure
    • Secondary Structure
    • Tertiary Structure
    • Quaternary Structure
  6. Formation of Peptides
  7. Protein Hydrolysis and Denaturation
  8. Enzymes and How They Work
    • Examples of Enzymes
    • Factors Affecting Enzyme Activity
    • Enzyme Inhibition
      Key Terms

Chapter 13: Carbohydrates

  1. Carbohydrates
  2. Monosaccharides
    • Common Hexoses
    • Common Pentoses
  3. Disaccharides
  4. Polysaccharides
  5. Sugar Structures and Representations
    • Fischer and Haworth Projections
    • Functional Groups in Monosaccharides
    • Polarimetric Measurements
    • D- and L-Sugars
    • Chirality
    • Conversion Between Representations
    • Cyclization of Glucose
  6. Reactions of Monosaccharides
    • Redox Reactions
    • Oxidation and Reduction
    • Reducing and Nonreducing Sugars
    • Benedict’s Reagent
    • Glycosidic Bond Formation
    • Other Carbohydrate Reactions
  7. Anomers and Enantiomers
  8. Carbohydrate Metabolism and Pathways
    • Natural Sources and Photosynthesis
    • Blood and Urine Glucose Tests
    • Galactosemia and Lactose Intolerance
      Key Terms

Chapter 14: Lipids

  1. Structure of Lipids
  2. Fatty Acids
    • Nomenclature of Fatty Acids
  3. Triglycerides and Reactions
    • Hydrolysis of Triglycerides
    • Lipase-Catalyzed Hydrolysis
    • Acid-Catalyzed Hydrolysis
    • Base-Catalyzed Hydrolysis
    • Hydrogenation
    • Oxidation
    • Fats, Oils, and Waxes
  4. Glycerophospholipids (Phospholipids)
    • Structure
    • Properties
  5. Cholesterol, Bile Salts, and Hormones
    • Steroid Hormones
  6. Cell Membranes
  7. ATP and Energy Production
    Key Terms

Chapter 15: Nucleic Acids and Protein Synthesis

  1. Nucleosides and Nucleotides
    • Nucleosides
    • Nucleotides
  2. Structure of Nucleic Acids
    • Primary Structure
    • Secondary Structure
    • RNA Structures
  3. DNA and Transcription
    • Prokaryotic Transcription
    • Eukaryotic Transcription
  4. DNA Replication
  5. Recombinant DNA and PCR
    • Polymerase Chain Reaction
  6. The Genetic Code
  7. Viruses
    • Viral Life Cycle
    • Viral Mutation and Evolution
      Key Terms

Appendices
Appendix 1: Periodic Tables
Appendix 2: Common Functional Groups and Subspecies
Appendix 3: VSEPR Theory and Molecular Geometries
Appendix 4: Units and Conversion Factors
Appendix 5: Common Anions and Cations
Appendix 6: Krebs Cycle

Julian Davis

Julian Davis, Ph.D. is a Professor of Organic Chemistry at the University of the Incarnate Word. He earned a B.S. in Chemistry with honors from North Carolina State University, followed by an M.A. and Ph.D. in Chemistry from the University of Texas at Austin. Following his graduate studies, Dr. Davis worked as a Research Scientist with Texas Fluorescence (TefLabs) and later served as a Teaching Post-Doctoral Associate at St. Edward’s University in Austin, Texas. He joined the faculty at the University of the Incarnate Word in 2006, where he continues to contribute to undergraduate chemistry education and instruction in organic chemistry.

Alicia Howard

Dr. Howard joined The University of Incarnate Word as an adjunct professor in 2018 and became a full-time Instructor for the Department of Chemistry and Biochemistry in 2021. Prior to becoming full-time in 2021, she worked as an adjunct professor for Northwest Vista College in the Natural Science Department. Dr. Howard graduated with her Doctorate in Chemistry from Texas Tech University in 2016 with an interest in drug design for ergosterol-dependent infectious diseases. She is currently working on implementing a CUREs, Course-Based Undergraduate Research Experience, based on the Malate Dehydrogenase Enzyme for the Biochemistry I Lab. A certified FLIGHT Mentor with over ten years of teaching experience in chemistry, she has a strong passion to inspire, encourage and connect to the younger generation.

This textbook provides a comprehensive foundation in health sciences and chemistry, beginning with the essential principles of scientific measurement and progressing through the structure and behavior of matter. Early chapters introduce key topics such as significant figures, scientific notation, unit conversions, precision and accuracy, and the classification of measurement systems. The text then builds toward a deeper understanding of atomic structure, the periodic table, chemical bonding, energy and matter, and the properties of solutions and chemical reactions, establishing a strong conceptual and quantitative base for scientific study.

In its later chapters, the book transitions into a detailed exploration of organic and biochemistry, including acids and bases, hydrocarbons, functional groups, biomolecules (such as carbohydrates, lipids, proteins, and nucleic acids), and metabolic processes. It also covers enzymes, cellular energy production, and genetic principles such as DNA replication, transcription, and protein synthesis. Supporting appendices provide reference materials on periodic trends, functional groups, molecular geometry, common ions, and biochemical cycles. 

Chapter 1: The Units of Measurements in Health Sciences

  1. The Scientific Method and Precise Measurements
  2. Significant Figures: Mastering Precision in Scientific Measurements
    • Examples
  3. How to Round Numbers
  4. Calculating Results with Significant Figures
  5. Significant Figures in Addition/Subtraction and Multiplication/Division
    • Addition and Subtraction
    • Multiplication and Division
  6. Scientific Notation
    • Performing Calculations Using Scientific Notation
  7. Measured Numbers
  8. Precision and Accuracy: Cornerstones of Reliable Chemistry
    • High Precision–High Accuracy
    • High Precision–Low Accuracy
    • Low Precision–High Accuracy
    • Low Precision–Low Accuracy
  9. The Units of Measurement
  10. Conventional (British or Imperial) Units
  11. Metric Units
  12. Scientific Units (SI)
  13. Converting Units
  14. Conversion Factors from One Unit to Another
  15. Base and Derived Units
  16. Mass, Volume, and Density
  17. Temperature Scales: °C, °F, and K
  • Celsius Scale (°C)
  • Fahrenheit Scale (°F)
  • Kelvin Scale (K)
  1. Health Notes
    Key Terms

Chapter 2: Atoms, Elements, Compounds, and Mixtures

  1. Atoms, Elements, Compounds, and Mixtures
  2. Physical and Chemical Properties
  3. Types of Mixtures (Homogeneous and Heterogeneous) and Separation Techniques
  4. Organization and Structure of the Periodic Table
  5. Key Information Provided by the Periodic Table
  6. Atomic Number and Atomic Mass
  7. Element Symbols and Names
    • Uranium (U)
    • Einsteinium (Es)
    • Californium (Cf)
    • Sodium (Na)
    • Special Note
  8. Periodic Trends and Element Properties
    • Ionization Energy and Electronegativity
    • Metallic and Nonmetallic Character
    • Reactivity and Group Trends
    • Ionic Sizes
    • Electrolytes and Biochemical Processes
  9. Writing Lewis (Dot) Structures
    • Valence Electrons
  10. Atomic Number, Protons, and Electrons
  • Hydrogen Example
  • Oxygen Example
  1. Avogadro’s Number and the Mole
  2. Mole Conversions (Particles and Mass)
  • Moles to Particles
  • Particles to Moles
  • Moles to Mass
  • Mass to Moles
    Key Terms

Chapter 3: Types of Chemical Bonds

  1. Covalent Bonds and the Octet Rule
    • Covalent Bonds
    • Octet Rule
    • Examples
  2. Lewis Structures
    • Basics
    • Construction
  3. Naming Molecules
    • Rules
    • Examples
  4. Single, Double, and Triple Bonds
  5. Ionic Bonds
    • Examples
  6. Electronegativity and Polar Bonds
    • Characteristics
    • Examples
  7. Polyatomic Ions
    • Examples
  8. Ionic Compound Formulas
    • Rules
  9. Covalent vs Ionic Compounds
  10. Transition Metal Compounds
  11. Metallic Bonds
    Key Terms

Chapter 4: Energy and Matter

  1. Matter, Heat, and Energy
    • Energy and Chemical Reactions
    • Units of Energy
    • Measurement of Energy Content
  2. States of Matter (Solid, Liquid, Gas, Plasma)
  3. Changes in Physical State
    • Phase Diagrams and Cooling Curves
  4. Properties of Gases and Gas Laws
  5. Attractive Forces
  6. Solutions and Dissolving
  7. Renewable and Sustainable Energy
    Key Terms

Chapter 5: Concentrations of Solutions

  1. Solutions
  2. Electrolytes and Nonelectrolytes
  3. Solubility
  4. Factors Affecting Solubility (T, P, Polarity)
    • Temperature
    • Pressure
    • Polarity
    • Applications
    • Saturated, Unsaturated, Supersaturated Solutions
  5. Percent Concentration
  6. Molarity (M) and Molality (m)
  7. Equivalents
  8. Dilution of Solutions
  9. Osmosis and Dialysis
  10. Tonicity
  • Colligative Properties
    Key Terms

Chapter 6: Chemical Reactions

  1. Writing Chemical Equations
  2. Balancing Chemical Equations
    • Steps 1–4
  3. Molar Mass
    • Examples
  4. Mass–Mole Relations
  5. Chemical Reaction Calculations
  6. Enthalpy Changes and Energy Diagrams
    • Endothermic Reactions
  7. Reaction Rate and Catalysts
    Key Terms

Chapter 7: Acids and Bases

  1. Self-Ionization of Water
  2. Properties of Acids and Bases
    • Broader Definitions
  3. Weak Acid/Base Equilibrium Constants
  4. pH Scale
  5. Acid–Base Reactions
  6. Conjugate Acids and Bases
  7. Buffers
    • Henderson–Hasselbalch Equation
      Key Terms

Chapter 8: Introduction to Organic Chemistry

  1. Hydrocarbons
  2. Elements in Organic Molecules (C, H, O, N)
    • Carbon
    • Hydrogen
    • Oxygen
    • Nitrogen
  3. Alkanes
  4. Linear, Branched, and Cyclic Alkanes
    • Skeletal Representation
  5. Geometry of Alkanes
    • Alkyl Groups
  6. Nomenclature of Alkanes
  7. Alkenes
  8. Geometry of Alkenes
  9. Cis-Trans Isomers
  10. Aromatic Compounds
  11. Alkene Nomenclature
  12. Alkynes
  13. Geometry of Alkynes
  14. Alkynes Nomenclature
  15. Hydrocarbon Properties
  • Environmental Impact
    Key Terms

Chapter 9: Alcohols, Ethers, Thiols, and Phenols

  1. Alcohols: Structure and Characteristics
  2. Alcohol Nomenclature
    • IUPAC Rules
    • Classification
  3. Chirality
  4. Hydration of Alkenes
  5. Dehydration of Alcohols (Zaitsev’s Rule)
  6. Ether Formation (Condensation Reactions)
  7. Thiols and Phenols
  8. Physical Properties of Functional Groups
    Key Terms

Chapter 10: Carbonyl Compounds and Redox Reactions

  1. Carbonyl Compounds
  2. Aldehydes and Ketones
  3. Nomenclature and Properties
    • Aldehydes
    • Ketones
    • Physical Properties
  4. Oxidation and Reduction Reactions
    • Oxidation
    • Reduction
  5. Addition Reactions
  6. Carboxylic Acids and Esters
  7. Reactions of Carboxylic Acids
    • Emulsification, Saponification, Surfactants
  8. Physical Properties of Acids and Esters
  9. Biological Redox Reactions
  10. Thioesters and Phosphoesters in Biology
    Key Terms

Chapter 11: Amines and Amides

  1. Nitrogen in the Environment and Organic Compounds
  2. Naming Simple Amines and Amides
  3. Types of Amines
    • Physical Properties of Amines
  4. Alkaloids
  5. Amines as Bases
    • Quaternary Ammonium Salts
  6. Neurotransmitters
  7. Vitamins
  8. Amino Acids
  9. Amides
  10. Hydrolysis of Amides
  11. Nitrogen-Containing Plastics and Polymers
    Key Terms

Chapter 12: Amino Acids, Proteins, and Enzymes

  1. General Structure of Amino Acids
  2. Acid-Base Characteristics of Amino Acids
  3. Essential Amino Acids
  4. Proteins
  5. Protein Structure (Primary, Secondary, Tertiary, Quaternary)
    • Primary Structure
    • Secondary Structure
    • Tertiary Structure
    • Quaternary Structure
  6. Formation of Peptides
  7. Protein Hydrolysis and Denaturation
  8. Enzymes and How They Work
    • Examples of Enzymes
    • Factors Affecting Enzyme Activity
    • Enzyme Inhibition
      Key Terms

Chapter 13: Carbohydrates

  1. Carbohydrates
  2. Monosaccharides
    • Common Hexoses
    • Common Pentoses
  3. Disaccharides
  4. Polysaccharides
  5. Sugar Structures and Representations
    • Fischer and Haworth Projections
    • Functional Groups in Monosaccharides
    • Polarimetric Measurements
    • D- and L-Sugars
    • Chirality
    • Conversion Between Representations
    • Cyclization of Glucose
  6. Reactions of Monosaccharides
    • Redox Reactions
    • Oxidation and Reduction
    • Reducing and Nonreducing Sugars
    • Benedict’s Reagent
    • Glycosidic Bond Formation
    • Other Carbohydrate Reactions
  7. Anomers and Enantiomers
  8. Carbohydrate Metabolism and Pathways
    • Natural Sources and Photosynthesis
    • Blood and Urine Glucose Tests
    • Galactosemia and Lactose Intolerance
      Key Terms

Chapter 14: Lipids

  1. Structure of Lipids
  2. Fatty Acids
    • Nomenclature of Fatty Acids
  3. Triglycerides and Reactions
    • Hydrolysis of Triglycerides
    • Lipase-Catalyzed Hydrolysis
    • Acid-Catalyzed Hydrolysis
    • Base-Catalyzed Hydrolysis
    • Hydrogenation
    • Oxidation
    • Fats, Oils, and Waxes
  4. Glycerophospholipids (Phospholipids)
    • Structure
    • Properties
  5. Cholesterol, Bile Salts, and Hormones
    • Steroid Hormones
  6. Cell Membranes
  7. ATP and Energy Production
    Key Terms

Chapter 15: Nucleic Acids and Protein Synthesis

  1. Nucleosides and Nucleotides
    • Nucleosides
    • Nucleotides
  2. Structure of Nucleic Acids
    • Primary Structure
    • Secondary Structure
    • RNA Structures
  3. DNA and Transcription
    • Prokaryotic Transcription
    • Eukaryotic Transcription
  4. DNA Replication
  5. Recombinant DNA and PCR
    • Polymerase Chain Reaction
  6. The Genetic Code
  7. Viruses
    • Viral Life Cycle
    • Viral Mutation and Evolution
      Key Terms

Appendices
Appendix 1: Periodic Tables
Appendix 2: Common Functional Groups and Subspecies
Appendix 3: VSEPR Theory and Molecular Geometries
Appendix 4: Units and Conversion Factors
Appendix 5: Common Anions and Cations
Appendix 6: Krebs Cycle

Julian Davis

Julian Davis, Ph.D. is a Professor of Organic Chemistry at the University of the Incarnate Word. He earned a B.S. in Chemistry with honors from North Carolina State University, followed by an M.A. and Ph.D. in Chemistry from the University of Texas at Austin. Following his graduate studies, Dr. Davis worked as a Research Scientist with Texas Fluorescence (TefLabs) and later served as a Teaching Post-Doctoral Associate at St. Edward’s University in Austin, Texas. He joined the faculty at the University of the Incarnate Word in 2006, where he continues to contribute to undergraduate chemistry education and instruction in organic chemistry.

Alicia Howard

Dr. Howard joined The University of Incarnate Word as an adjunct professor in 2018 and became a full-time Instructor for the Department of Chemistry and Biochemistry in 2021. Prior to becoming full-time in 2021, she worked as an adjunct professor for Northwest Vista College in the Natural Science Department. Dr. Howard graduated with her Doctorate in Chemistry from Texas Tech University in 2016 with an interest in drug design for ergosterol-dependent infectious diseases. She is currently working on implementing a CUREs, Course-Based Undergraduate Research Experience, based on the Malate Dehydrogenase Enzyme for the Biochemistry I Lab. A certified FLIGHT Mentor with over ten years of teaching experience in chemistry, she has a strong passion to inspire, encourage and connect to the younger generation.