Pion beta decay changes a charged pion into a neutral pion and a lepton pair through the weak charged current. The small charged-neutral pion mass gap severely restricts phase space, giving an approximately fifth-power dependence on that gap. It does not have the charged-lepton mass suppression of direct leptonic pion decay.

A device that amplifies a particle signal through repeated production of secondary electrons.

In a one-dimensional identical-particle model, a contact interaction has two-body potential $U(x,x^{\prime })=g\delta (x-x^{\prime })$, using the Dirac delta distribution. For bosons, its second quantization is the displayed normally ordered Hamiltonian operator. Projection onto orthonormal modes gives $H_{\mathrm{int}}=(g/2){\sum }_{ijkl}{I}_{ijkl}{a}_i^{†}{a}_j^{†}{a}_k{a}_l$, where $I_{ijkl}=\int {\phi }_i^{\ast }{\phi }_j^{\ast }{\phi }_k{\phi }_{l}dx$. The overlap integrals determine which mode-changing processes survive. A finite-mode model describes that projection; discarded modes can still matter to the full physical system.

An attosecond is one quintillionth of a second.

For the Schwarzschild metric with $\mu =GM/c^2$, let $k=(1-2\mu /r)\dot{t}$ and $h=r^2\dot{\varphi }$ on an equatorial timelike geodesic. The normalization of the four-velocity gives ${\dot{r}}^2+V(r)=c^2(k^2-1)$, where $V(r)=(1-2\mu /r)h^2/r^2-2\mu c^2/r$. A circular geodesic obeys $V^{\prime }(R)=0$, giving the displayed constants and requiring $R>3\mu$. Its coordinate angular velocity is ${\Omega }^2=GM/R^3$, and its proper clock rate is $d\tau /dt=\sqrt{1-3\mu /R}$. Differentiating $V$ twice at the circular solution gives stability for $R>6\mu$.

Raman scattering is inelastic scattering of light in which the outgoing photon has a different frequency because matter gains or loses internal energy. Molecular vibration is a particularly useful recipient: a visible photon can reveal an internal energy spacing normally associated with infrared frequencies. Rayleigh scattering supplies the much stronger, approximately unchanged-frequency reference. The distinction concerns the transferred energy, rather than merely a change of direction or the colour of the illuminating beam.

The elementary bookkeeping is conservation of energy:Here $h$ is the Planck constant, ${\nu }_0$ and ${\nu }_s$ are the incident and scattered photon frequencies, and $E_i,E_f$ are initial and final internal molecular energies. This expression neglects translational recoil and Doppler broadening; those can matter in sufficiently precise gas measurements. A positive internal energy change gives Stokes Raman scattering, and a negative one gives Anti-Stokes Raman scattering. The energy difference determines a possible line position, but it does not by itself establish that a transition is optically allowed or predict its strength.

The spontaneous molecular process developed here has a connection to the Raman transition used in atomic measurement methods: two photon interactions transfer an internal energy difference. Coherently driving that process with two applied light fields is a different experimental regime from collecting weak spontaneous Raman scattering beside an illuminating beam.

A triglyceride contains three ester linkages joining glycerol to fatty acid-derived acyl groups. Complete saponification therefore consumes three hydroxide equivalents per triglyceride, yielding one glycerol and three fatty acid carboxylates.^[ref]

Writing the three hydrocarbon groups separately allows their compositions to differ:This is the preceding ester chemical equation applied three times: each linkage supplies one carboxylate, and each formerly esterified oxygen on the glycerol scaffold gains one hydrogen. The two sides retain the same three ${\mathrm{R}}_i$ groups and have net electric charge $-3$.

Soap consists of sodium or potassium salts of long-chain fatty acids. Its carboxylate head is hydrophilic, while its long hydrocarbon tail is hydrophobic. This makes it an amphiphile and a surfactant: the tails can associate with grease while the heads remain exposed to water, helping disperse grease for rinsing. An acetate ion is also a carboxylate, but lacks the long hydrophobic tail that gives soap this cleaning role.^[ref]

Consider a hypothetical closed, well mixed chemical solution initially containing $20\mathrm{mmol}$ of ethyl acetate, $12\mathrm{mmol}$ of hydroxide, and no acetate ions or ethanol. One millimole is $10^{-3}$ mole. Assume complete conversion as far as the one-to-one chemical equation allows, with no competing chemical reactions. This is an ideal stoichiometry calculation, not a measured yield.

Let the extent of reaction be $\xi$, expressed in millimoles. The four values of amount of substance, in the order ethyl acetate, hydroxide, acetate ion, ethanol, areThe upper bound follows because both reactant quantities must be nonnegative. Thus hydroxide is the limiting reagent, and the ideal endpoint $\xi =12$ leavesThe carboxylate formed equals the hydroxide consumed, while unreacted ester remains. Adding more hydroxide raises the stoichiometry bound; merely waiting longer does not change that bound. To convert these values of amount of substance into concentrations, a volume is also required. The endpoint does not specify the reaction rate or time needed to approach it.