Utilisateur
A species that increases reaction rate by providing a lower activation energy pathway and is regenerated (not consumed overall).
Because the catalyst is reused (high turnover), so one catalyst molecule can produce many product molecules.
No. It only helps the system reach equilibrium faster (speeds forward + reverse).
How well a reaction converts reactant atoms into the desired product (less waste = higher atom economy). Few/no byproducts → most atoms end up in the product.
Solvents are often the largest source of waste, so reusing or avoiding solvents improves sustainability.
Biological reactions are too slow under normal conditions; enzymes catalyze them so life can function at mild temperatures/pH.
Transition metals can switch oxidation states, bind substrates strongly, and stabilize reactive intermediates → enabling fast/selective catalysis.
Mostly yes indirectly, but some ecosystems (thermal vents) use chemosynthesis driven by inorganic chemical energy, not sunlight.
Many molecules have two enantiomers (mirror-image forms) that can behave differently biologically. Life uses mostly one enantiomer form (e.g., mostly L-amino acids), suggesting a common origin event.
Abiotic synthesis is usually non-selective, producing racemic mixtures without biological selection/catalysis.
Industrial process making H₂ from natural gas using steam + heat + catalyst.
CH₄ + 2H₂O → CO₂ + 4H₂
It’s currently the most cost-effective large-scale method to produce hydrogen. Upgrading crude oil (hydrotreating/hydrocracking) to produce cleaner hydrocarbons.
CH₄ has strong greenhouse effect, so leaks can greatly increase the total emissions footprint.
Converting atmospheric N₂ into NH₃ (ammonia) for fertilizer production.
N₂ + 3H₂ ⇌ 2NH₃
It enabled large-scale fertilizer production, sustaining ~30–50% of the global population.
Much of the nitrogen in human proteins originated as atmospheric N₂ fixed into fertilizer via H-B.
Ammonium sulfate, (NH₄)₂SO₄ (plus others like urea, ammonium nitrate).
The required H₂ is commonly made by steam reforming methane, producing CO₂.
It reduced reliance on imported nitrates during the nitrate blockade by producing ammonia domestically.
H₂ from methane steam reforming with CO₂ released to atmosphere.
H₂ from methane steam reforming with CO₂ captured + geologically sequestered (CCS).
H₂ from electrolysis of water powered by low-carbon electricity.
CH₄ + 2H₂O → CO₂ + 4H₂
Naturally occurring underground H₂ formed by geologic redox processes (e.g., Fe oxidation + H⁺ reduction).
It could provide low-carbon H₂ without CO₂ emissions or large electricity input, reducing need for CCS/electrolysis infrastructure.
~1°C warming has been primarily caused by human-made greenhouse gas emissions, especially CO₂.
It’s a major greenhouse gas from energy + industry and it accumulates in the atmosphere.
PFAS compounds that are extremely stable and persist for decades in the environment.
Per- and polyfluoroalkyl substances.
They have low friction, repel water/oil, and are heat/chemically stable. Fire-fighting foams, non-stick coatings, stain/water-resistant fabrics (also food packaging liners).
The carbon chain is fully fluorinated (all possible H replaced by F).
The C–F bond is extremely strong, so PFAS resist degradation reactions. Fluorinated surfaces have very low surface energy and weak intermolecular attractions → liquids don’t wet the surface.
They persist, spread globally, and some are toxic at low concentrations and can accumulate.
The photoelectric effect (electrons ejected by light above a threshold energy).
Electron diffraction patterns from crystals.
λ= h/ mv
Particles (especially electrons) can have a measurable wavelength, enabling diffraction.
The kinetic energy of photoelectrons ejected from a surface to determine binding energies (element + chemical state).
Photon energy is converted into binding energy + kinetic energy (plus work function in XPS).
ΔxΔp≥ h/4 π
Electrons can’t have exact position + momentum → they must be described by probability/orbitals, not classical paths.
Because electrons behave like waves, so atomic structure must be described using wave mechanics (not classical particle mechanics).
A mathematical function that describes the electron’s quantum state (wave behavior in an atom).
The probability density of finding the electron at a given position.
The allowed wavefunctions (orbitals) and their corresponding energies.
Only certain standing wave solutions are allowed in atoms → discrete energies.
Like a vibrating string: only wave patterns that “fit” are stable → allowed orbitals.
It explains discrete orbital energies; electrons are ejected only if photon energy exceeds binding energy (measured in XPS).
ite the simplified Schrödinger equation.
^
HΨ=EΨ
The total energy operator
^
T
+
^
V
Allowed energies (E) and wavefunctions/orbitals (Ψ) → orbital shapes.
Probability density of finding the electron at a position.
Single-valued, finite, continuous/smooth, and normalizable.
H has only one electron (2-body). He has electron–electron repulsion, making it a many-body problem.
Use approximations (hydrogen-like orbitals + effective nuclear charge / average field).
Because hydrogen’s potential depends only on distance r, so the system is spherically symmetric.
Ψ(r,θ,ϕ)=R(r)P(θ)F(ϕ)
Principal energy level/size; n = 1,2,3…
Orbital angular momentum / orbital shape; ℓ = 0 to n−1
orbital orientation; mℓ= -ℓ, ..., + ℓ
ℓ=0 s, ℓ=1 p, ℓ=2 d, ℓ=3 f.
3s, 3p, 3d.
