Every biological process you'll encounter in this course—from how your cells extract energy from glucose to how your body builds the proteins that make you you—comes down to a handful of core reaction types. You're not just memorizing reactions here; you're learning the chemical logic that explains metabolism, energy transfer, homeostasis, and genetic continuity. When you understand why hydrolysis breaks bonds while condensation builds them, or why electrons flowing through redox reactions power your mitochondria, you're thinking like a biochemist.
The exam will test whether you can connect specific reactions to their biological functions and compare mechanisms across different contexts. Don't just memorize that ATP hydrolysis releases energy—know why breaking that phosphate bond matters and how it relates to the broader theme of energy coupling in cells. Master the underlying principles, and you'll be ready for anything from multiple choice to FRQ-style applications.
Bond-Breaking and Bond-Making Reactions
These complementary reactions control how biological macromolecules are assembled and disassembled. The key mechanism is water—either added to break bonds or removed to form them.
Hydrolysis Reactions
Water addition breaks covalent bonds—the H and OH from water attach to the fragments, cleaving the original molecule
Essential for digestion of all macromolecules: proteins → amino acids, polysaccharides → monosaccharides, lipids → fatty acids and glycerol
ATP hydrolysis (ATP+H2O→ADP+Pi) releases approximately 30.5 kJ/mol, powering cellular work
Condensation Reactions
Dehydration synthesis joins monomers by removing water—one molecule donates OH, the other donates H
Builds all biological polymers: peptide bonds link amino acids, glycosidic bonds link sugars, phosphodiester bonds link nucleotides
Energetically unfavorable on its own—requires coupling to ATP hydrolysis to proceed in cells
Compare: Hydrolysis vs. Condensation—both involve water and covalent bonds, but they're exact opposites. Hydrolysis uses water to break bonds (catabolic), while condensation releases water to form bonds (anabolic). If an FRQ asks how polymers are built and broken, this pair is your answer.
Electron Transfer Reactions
Redox reactions are the engine of cellular energy production. Electrons carry energy, and controlling their flow allows cells to capture that energy in usable forms.
Oxidation-Reduction (Redox) Reactions
Electron transfer changes oxidation states—the molecule losing electrons is oxidized (OIL: Oxidation Is Loss), the one gaining is reduced (RIG: Reduction Is Gain)
Powers both cellular respiration and photosynthesis—electron carriers like NAD+/NADH and FAD/FADH2 shuttle electrons between reactions
Drives the electron transport chain—stepwise electron transfer creates the proton gradient that produces most cellular ATP
Krebs Cycle (Citric Acid Cycle)
Oxidizes acetyl-CoA (C2) completely to CO2 through eight enzymatic steps in the mitochondrial matrix
Generates electron carriers: each turn produces 3 NADH, 1 FADH2, and 1 GTP (equivalent to ATP)
Metabolic hub connecting carbohydrate, lipid, and protein catabolism—intermediates enter and exit for biosynthesis
Compare: Glycolysis vs. Krebs Cycle—both are central metabolic pathways, but glycolysis occurs in the cytoplasm and partially oxidizes glucose (producing pyruvate), while the Krebs cycle occurs in mitochondria and completes oxidation to CO2. Know which produces more electron carriers (Krebs wins).
Proton Transfer and Phosphate Group Reactions
These reactions regulate cellular activity through chemical signaling and pH control. Protons and phosphate groups act as molecular switches.
Acid-Base Reactions
Proton (H+) transfer between molecules—acids donate protons, bases accept them (Brønsted-Lowry definition)
Buffer systems maintain homeostasis—the bicarbonate buffer (H2CO3/HCO3−) keeps blood pH near 7.4
Enzyme activity depends on pH—protonation states of amino acid side chains determine protein shape and function
Phosphorylation Reactions
Addition of phosphate group (PO43−) changes a molecule's charge, shape, and activity—often acts as an on/off switch
ATP is the universal phosphate donor—kinases transfer phosphate to substrates, phosphatases remove it
Signal transduction cascades rely on sequential phosphorylation to amplify and transmit cellular signals
Compare: Acid-base vs. Phosphorylation—both involve transfer of charged species that alter molecular behavior, but acid-base reactions transfer H+ (affecting pH and protonation), while phosphorylation transfers PO43− (affecting activity and signaling). Both are reversible regulatory mechanisms.
Energy Conversion Pathways
These multi-step processes transform energy between different chemical forms. They represent the integration of multiple reaction types working together.
Glycolysis
Ten-step pathway converts one glucose (C6H12O6) into two pyruvate (C3H4O3) molecules in the cytoplasm
Net yield: 2 ATP (substrate-level phosphorylation) and 2 NADH—occurs with or without oxygen
Investment phase uses 2 ATP; payoff phase generates 4 ATP—understanding this split is frequently tested
Photosynthesis
Light-dependent reactions in thylakoid membranes split water, release O2, and generate ATP + NADPH via electron transport
Calvin cycle (light-independent) in the stroma uses ATP and NADPH to fix CO2 into glucose: 6CO2+6H2OlightC6H12O6+6O2
Reverses cellular respiration energetically—stores light energy in chemical bonds rather than releasing it
Compare: Glycolysis vs. Photosynthesis—glycolysis breaks down glucose to release energy (catabolic), while photosynthesis builds glucose to store energy (anabolic). Both involve redox reactions and phosphorylation, but energy flows in opposite directions.
Information Transfer Reactions
These reactions ensure genetic information is accurately copied and expressed. The chemistry of nucleic acids underlies heredity and protein production.
DNA Replication
Semi-conservative mechanism—each new double helix contains one original strand and one newly synthesized strand
DNA polymerase adds nucleotides to the 3′ end, forming phosphodiester bonds via condensation reactions
High fidelity maintained through complementary base pairing (A-T, G-C) and proofreading—error rate approximately 10−9
Protein Synthesis
Transcription in the nucleus: RNA polymerase builds mRNA from DNA template using condensation reactions
Translation at ribosomes: tRNA delivers amino acids, peptide bonds form between them (also condensation)
Central dogma (DNA → RNA → Protein) represents the flow of genetic information in all cells
Compare: DNA Replication vs. Protein Synthesis—both use template-directed synthesis and condensation reactions, but replication copies DNA for cell division (information preservation), while protein synthesis expresses DNA as functional proteins (information utilization). Both require high accuracy but serve different purposes.
Quick Reference Table
Concept
Best Examples
Bond breaking with water
Hydrolysis, ATP hydrolysis, digestion
Bond forming with water release
Condensation, peptide bond formation, glycosidic bonds
Electron transfer
Redox reactions, Krebs cycle, electron transport chain
Proton transfer
Acid-base reactions, buffer systems
Phosphate group transfer
Phosphorylation, ATP → ADP, kinase activity
Glucose catabolism
Glycolysis, Krebs cycle
Energy storage from light
Photosynthesis, Calvin cycle
Genetic information flow
DNA replication, protein synthesis
Self-Check Questions
Which two reaction types are exact opposites involving water, and how do they relate to building versus breaking macromolecules?
Both glycolysis and the Krebs cycle are central metabolic pathways—compare their locations, oxygen requirements, and primary products.
If a cell needs to activate an enzyme quickly without synthesizing new protein, which reaction type would most likely be involved, and why?
Explain how redox reactions connect photosynthesis and cellular respiration. Which process oxidizes water, and which reduces oxygen?
FRQ-style: A mutation prevents a cell from performing condensation reactions. Predict the effects on (a) protein synthesis, (b) DNA replication, and (c) ATP production. Justify each prediction with specific reaction mechanisms.