Chapter 2: The Chemical Basis of Life - Water & Carbon

Page 1: Chemical Basis of Life

Chapter 2 BY111: The Chemical Basis of Life: Water & Carbon.

Page 2: Essential Elements

Four elements make up 96%96\% of all matter in organisms: Hydrogen, Oxygen, Carbon, and Nitrogen. Core concept: form follows function.

Page 3: Basic Atomic Structure

  • Protons: Positively (++) charged particles located in the nucleus.

  • Neutrons: Neutral particles located in the nucleus.

  • Electrons: Negatively (-) charged particles in orbitals surrounding the nucleus.

Page 4: Atomic Number

  • Atomic Number: The characteristic number of protons in an atom's nucleus.

  • Atoms with the same atomic number share chemical properties and belong to the same element (e.g., Helium 24He{}_2^4\text{He} has an atomic number of 22).

Page 5: Isotopes and Mass Number

  • Isotopes: Forms of an element with different numbers of neutrons.

  • Mass Number: Total number of protons plus neutrons of the most common isotope.

Page 6: Atomic Notation

Atomic notation displays the mass number (protons + neutrons) above the atomic number (protons) beside the atomic symbol.

Page 7: Subatomic Particle Calculations

For Carbon (612C{}_6^{12}\text{C}):

  • Atomic number 6=6 protons=6 electrons6 = 6\text{ protons} = 6\text{ electrons}.

  • Mass number 12=protons+neutrons12 = \text{protons} + \text{neutrons}.

  • Number of neutrons: 126=612 - 6 = 6.

Page 8: Valence Shells

  • Valence: The number of unpaired electrons in an atom's outer electron shell.

  • Determines chemical bonding potential.

Page 9: Chemical Bonding

  • Atoms are most stable when each electron orbital is filled.

  • Covalent Bond: Unpaired valence electrons are shared by both nuclei.

  • Ionic Bond: Electrons are transferred completely from one atom to another.

Page 10: Covalent Bonding in Hydrogen

Two hydrogen atoms share unpaired valence electrons to form a molecular hydrogen (H2\text{H}_2) covalent bond.

Page 11: Covalent Bonding in Water and Oxygen

  • Two oxygen atoms covalently bond to form oxygen gas (O2\text{O}_2).

  • One oxygen atom covalently bonds with two hydrogen atoms to form water (H2O\text{H}_2\text{O}).

Page 12: Polar vs Nonpolar Covalent Bonds

  • Nonpolar Covalent Bond: Electrons are shared equally between atoms (e.g., H2\text{H}_2).

  • Polar Covalent Bond: Electrons are shared unequally due to differences in electronegativity, creating partial charges (δ\delta^- on Oxygen, δ+\delta^+ on Hydrogen in H2O\text{H}_2\text{O}).

Page 13: Ions and Ionic Bonds

  • Ion: An atom or molecule carrying a charge.

  • Cation: Positively charged atom formed by losing an electron.

  • Anion: Negatively charged atom formed by gaining an electron.

  • Ionic Bond: Electrostatic attraction between oppositely charged ions.

Page 14: Formation of Sodium Chloride

  • Sodium loses an electron to form cation Na+\text{Na}^+.

  • Chlorine gains an electron to form anion Cl\text{Cl}^-.

  • Electrostatic attraction forms a table salt (NaCl\text{NaCl}) crystal.

Page 15: Chemical Bonding Spectrum

Chemical bonds exist on a continuum: Nonpolar covalent (equal sharing) \rightarrow Polar covalent (partial charges) \rightarrow Ionic (full charge transfer).

Page 16: Covalent Bond Types

  • Single Bonds: e.g., H2O\text{H}_2\text{O}, NH3\text{NH}_3, CH4\text{CH}_4

  • Double Bonds: e.g., CO2\text{CO}_2

  • Triple Bonds: e.g., N2\text{N}_2

Page 17: Molecular Representation Models

Molecules are represented using molecular formulas, structural formulas, ball-and-stick models, and space-filling models.

Page 18: Water Solvency and Electronegativity

  • Water is an effective solvent due to polar covalent bonds.

  • Electronegativity order: \text{O} > \text{N} > \text{C} = \text{H}.

  • Electronegativity increases with proton number and decreases with electron shielding.

Page 19: Hydrogen Bonding in Water

Polarity allows hydrogen bonds to form between partial positive hydrogen atoms and partial negative oxygen atoms of neighboring water molecules.

Page 20: Hydrophilic Interactions

  • Hydrophilic: Ions and polar molecules that interact with water's partial charges and remain in solution.

Page 21: Dissolution of Ionic Compounds

Water dissolves ionic crystals such as NaCl\text{NaCl} by surrounding individual Na+\text{Na}^+ and Cl\text{Cl}^- ions through charge interactions.

Page 22: Hydrophobic Interactions

  • Hydrophobic: Uncharged, nonpolar compounds that do not dissolve in water.

Page 23: Structural Attributes of Water

Water's unique features stem from its small size, bent shape, highly polar covalent bonds, and overall polarity.

Page 24: Properties of Water

Key properties driven by hydrogen bonding:

  • Cohesion and adhesion

  • Lower density as a solid than liquid

  • High capacity for energy absorption

Page 25: Cohesion, Adhesion, and Surface Tension

  • Cohesion: Binding between like molecules (water to itself), producing high surface tension.

  • Adhesion: Binding between unlike molecules.

  • Capillary Action: Result of combined cohesive and adhesive properties.

Page 26: Surface Tension Mechanisms

  • Adhesion pulls water upward at solid contact points to form a meniscus.

  • Surface cohesion resists upward pull, creating surface tension that supports light objects.

Page 27: Thermal Properties and Density of Water

  • Water expands upon freezing, making ice less dense than liquid water.

  • High specific heat and high heat of vaporization allow significant energy absorption.

Page 28: pH Scale

Solutions range on a spectrum from Acidic (high proton concentration) to Neutral to Basic (low proton concentration).

Page 29: Chemical Evolution Theory

  • Pattern: Complex carbon-containing substances are required for life.

  • Process: Simple chemical compounds combined early in Earth's history to form complex carbon molecules.

Page 30: Atmospheric Environments

Early atmospheric environments included volcanic gases: H2O\text{H}_2\text{O} vapor, CO2\text{CO}_2, N2\text{N}_2, and possibly H2\text{H}_2 and CO\text{CO}.

Page 31: Hydrothermal Vents

Deep-sea hydrothermal vents provided extreme heat, gases (CO2\text{CO}_2, H2\text{H}_2), and catalytic metals (nickel, iron).

Page 32: Chemical Equilibrium and Reactions

  • Reversible reaction example: CO2(g)+H2O(l)H2CO3(aq)\text{CO}_2(g) + \text{H}_2\text{O}(l) \rightleftharpoons \text{H}_2\text{CO}_3(aq).

  • Chemical Equilibrium: Occurs when forward and reverse reaction rates are equal.

  • Endothermic: Absorbs heat; Exothermic: Releases heat.

Page 33: Forms of Energy

  • Energy: Capacity to do work or supply heat.

  • Potential Energy: Stored energy.

  • Kinetic Energy: Energy of active motion.

Page 34: Reaction Spontaneity

Spontaneous reactions are determined by:

  1. Decreased potential energy in products.

  2. Increased entropy/disorder (lower order in products).

Example reaction: 2H2+O22H2O2\,\text{H}_2 + \text{O}_2 \rightarrow 2\,\text{H}_2\text{O} releases potential energy as heat and light.

Page 35: Cellular Energy Changes

Combustion / Cellular Respiration reaction:

C6H12O6+6O26CO2+6H2O+heat\text{C}_6\text{H}_{12}\text{O}_6 + 6\,\text{O}_2 \rightarrow 6\,\text{CO}_2 + 6\,\text{H}_2\text{O} + \text{heat}

Reactants have high potential energy and order; products have low potential energy and lower order.

Page 36: Pathways of Prebiotic Synthesis

Simple environmental molecules reacted via sunlight or hydrothermal vent catalysis to produce complex molecules like ribose, glycine, acetaldehyde, and acetic acid.

Page 37: Experimental Testing of Chemical Evolution

Miller-Urey spark discharge experiments demonstrated that adding kinetic energy (spark) to simple gases (CH4\text{CH}_4, NH3\text{NH}_3, H2\text{H}_2, water vapor) yields formaldehyde, hydrogen cyanide, and organic compounds containing C-C\text{C-C} bonds (amino acids).

Page 38: Precursor Synthesis

  • Key chemical evolution step: Formation of formaldehyde (H2CO\text{H}_2\text{CO} / CH2O\text{CH}_2\text{O}) and hydrogen cyanide (HCN\text{HCN}).

  • Reaction: CO2(g)+2H2(g)CH2O(g)+H2O(g)\text{CO}_2(g) + 2\,\text{H}_2(g) \rightarrow \text{CH}_2\text{O}(g) + \text{H}_2\text{O}(g).

Page 39: Free Radical Formation

High-energy photons break unreactive atmospheric molecules into highly reactive free radicals (H\text{H}, O\text{O}, CO\text{CO}) with unpaired electrons.

Page 40: Storage of Chemical Energy

Chemical energy is potential energy in bonds. Ancient solar energy was converted into stored chemical energy inside H2CO\text{H}_2\text{CO} and HCN\text{HCN}.

Page 41: Importance of Carbon

Carbon has 44 valence electrons and forms up to four covalent bonds, enabling complex molecular shapes essential for chemical evolution.

Page 42: Carbon Chains and Rings

Carbon forms diverse skeletal shapes, including chains (e.g., Octane, C8H18\text{C}_8\text{H}_{18}) and rings (e.g., Glucose, C6H12O6\text{C}_6\text{H}_{12}\text{O}_6).

Page 43: Function of Carbon Skeletons

Carbon atoms furnish the framework that gives organic molecules overall shape, while attached functional groups define reactivity.

Page 44: Six Major Functional Groups

  • Amino: Acts as a base; attracts a proton (e.g., Glycine).

  • Carboxyl: Acts as an acid; loses a proton (e.g., Acetic acid).

  • Carbonyl: Reacts to form larger compounds; found in aldehydes and ketones (e.g., Acetaldehyde, Acetone).

  • Hydroxyl: Highly polar; enhances solubility through hydrogen bonding; weak acid (e.g., Ethanol).

  • Phosphate: Multi-phosphate links store large chemical energy amounts (e.g., 3-Phosphoglyceric acid).

  • Sulfhydryl: Forms disulfide (S-S\text{S-S}) bonds to stabilize protein structure (e.g., Cysteine).