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  2. Proton nuclear magnetic resonance - Wikipedia

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

    The CH 2 peak will be split into a doublet by the CH peak—with one peak at 1 ppm + 3.5 Hz and one at 1 ppm − 3.5 Hz (total splitting or coupling constant is 7 Hz). In consequence the CH peak at 2.5 ppm will be split twice by each proton from the CH 2. The first proton will split the peak into two equal intensities and will go from one peak ...

  3. Hexamethylbenzene - Wikipedia

    en.wikipedia.org/wiki/Hexamethylbenzene

    The complete IUPAC name for this compound is 1,2,3,4,5,6-hexamethylbenzene. [18] The locants (the numbers in front of the name) are superfluous, however, as the name hexamethylbenzene uniquely identifies a single substance and thus is the formal IUPAC name for the compound. [19]

  4. 1,2,4,5-Tetrachloro-3-nitrobenzene - Wikipedia

    en.wikipedia.org/wiki/1,2,4,5-tetrachloro-3...

    1,2,4,5-Tetrachloro-3-nitrobenzene (tecnazene) is an organic compound with the formula HC 6 Cl 4 NO 2. It is a colorless solid. A related isomer is 1,2,3,4-tetrachloro-5-nitrobenzene. It is used as a standard for quantitative analysis by nuclear magnetic resonance. [4] [5]

  5. Magnetic inequivalence - Wikipedia

    en.wikipedia.org/wiki/Magnetic_inequivalence

    The same is true with respect to their coupling relationships with H-5. Similarly, H-4 and H-5 are chemically equivalent but magnetically inequivalent owing to their different coupling relationships with H-3 (or H-6). A classic example showing highly complex splitting is that of 1,2-dichlorobenzene. The two signals are nearly mirror-symmetrical.

  6. Simple aromatic ring - Wikipedia

    en.wikipedia.org/wiki/Simple_aromatic_ring

    Many simple aromatic rings have trivial names. They are usually found as substructures of more complex molecules ("substituted aromatics"). Typical simple aromatic compounds are benzene, indole, and pyridine. [1] [2] Simple aromatic rings can be heterocyclic if they contain non-carbon ring atoms, for example, oxygen, nitrogen, or sulfur.

  7. Tetramethylbenzene - Wikipedia

    en.wikipedia.org/wiki/Tetramethylbenzene

    The tetramethylbenzenes constitute a group of substances of aromatic hydrocarbons, which structure consists of a benzene ring with four methyl groups (–CH 3) as a substituent. [1] Through their different arrangement, they form three structural isomers with the molecular formula C 10 H 14. They also belong to the group of C 4-benzenes.

  8. 13 Things You Should Never, Ever Carry in Your Wallet - AOL

    www.aol.com/finance/13-things-never-ever-carry...

    Plus, were a thief to end up getting their hands on all of that at once, it would be terribly easy for them to unleash havoc on your bank account. Related: 6 Places You Should Never Keep Your Phone.

  9. 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.