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  2. Propyl propanoate - Wikipedia

    en.wikipedia.org/wiki/Propyl_propanoate

    Propyl propanoate (also known as propyl propionate and n-propyl propionate) is the organic compound with the molecular formula C 6 H 12 O 2. It is the ester of propanol and propionic acid. Like most esters, propyl propanoate is a colorless liquid with a fruity odor. The scent of propyl propionate is described as a chemically tinged pineapple or ...

  3. Proton nuclear magnetic resonance - Wikipedia

    en.wikipedia.org/wiki/Proton_nuclear_magnetic...

    There are three different types of H atoms in ethyl acetate regarding NMR. The hydrogens (H) on the CH 3 COO− group are not coupling with the other H atoms and appear as a singlet, but the −CH 2 − and −CH 3 hydrogens of the ethyl group (−CH 2 CH 3) are coupling with each other, resulting in a quartet and triplet respectively.

  4. Propionic acid - Wikipedia

    en.wikipedia.org/wiki/Propionic_acid

    The propionate / ˈ p r oʊ p i ə n eɪ t /, or propanoate, ion is C 2 H 5 COO −, the conjugate base of propionic acid. It is the form found in biological systems at physiological pH. A propionic, or propanoic, compound is a carboxylate salt or ester of propionic acid. In these compounds, propionate is often written in shorthand, as CH 3 CH ...

  5. Paramagnetic nuclear magnetic resonance spectroscopy

    en.wikipedia.org/wiki/Paramagnetic_nuclear...

    Paramagnetism diminishes the resolution of an NMR spectrum to the extent that coupling is rarely resolved. Nonetheless spectra of paramagnetic compounds provide insight into the bonding and structure of the sample. For example, the broadening of signals is compensated in part by the wide chemical shift range (often 200 ppm in 1 H NMR).

  6. Nuclear Overhauser effect - Wikipedia

    en.wikipedia.org/wiki/Nuclear_Overhauser_effect

    In the trans state proton {H} is far from the phenyl group showing blue coloured NOEs; while the cis state holds proton {H} in the vicinity of the phenyl group resulting in the emergence of new NOEs (show in red). Another example (bottom) where application where the NOE is useful to assign resonances and determine configuration is polysaccharides.

  7. List of esters - Wikipedia

    en.wikipedia.org/wiki/List_of_esters

    An ester of carboxylic acid.R stands for any group (organic or inorganic) and R′ stands for organyl group.. In chemistry, an ester is a compound derived from an acid (organic or inorganic) in which the hydrogen atom (H) of at least one acidic hydroxyl group (−OH) of that acid is replaced by an organyl group (−R).

  8. Triple-resonance nuclear magnetic resonance spectroscopy

    en.wikipedia.org/wiki/Triple-resonance_nuclear...

    Triple resonance experiments are a set of multi-dimensional nuclear magnetic resonance spectroscopy (NMR) experiments that link three types of atomic nuclei, most typically consisting of 1 H, 15 N and 13 C. These experiments are often used to assign specific resonance signals to specific atoms in an isotopically-enriched protein.

  9. Pentyl propanoate - Wikipedia

    en.wikipedia.org/wiki/Pentyl_propanoate

    Pentyl propanoate (also known as amyl propionate) is an organic ester formed by the condensation of pentan-1-ol and propanoic acid. [2] It is a colorless liquid with an apple-like odor, that floats on water.