「HYDROGEN」の共起表現一覧(1語右が「atoms」)
該当件数 : 104件
Hydrogen atoms on carbon are implicit. | |
The bridging | hydrogen atoms provide one electron each. |
In the chemical reactions, | hydrogen atoms on the hydrocarbon are replaced by chlo |
ed triplet corresponds to the terminal methyl | hydrogen atoms that experience spin-spin splitting fro |
corresponds to the more deshielded methylene | hydrogen atoms that are spin-spin split by the adjacen |
of dichloromethane (DCM, CH2Cl2) in which the | hydrogen atoms ("H") are replaced with deuterium (heav |
edH2 the reduced flavin (upon addition of two | hydrogen atoms) and FlH• the semiquinone form (additio |
ydrides have a defined standard population of | hydrogen atoms attached to a skeletal structure. |
With a cyclopentane-ring, it has two | hydrogen atoms less and thus is not an isomer. |
The compound is used as a source of | hydrogen atoms in organic synthesis. |
It is more ordered than ice VII, since the | hydrogen atoms assume fixed positions. |
The compound consists of methane wherein two | hydrogen atoms are replaced by two phenyl groups. |
Two | hydrogen atoms in the complex can be replaced by sodiu |
Watson-Crick base pairs in a siRNA ( | hydrogen atoms are not shown) |
In the example, atoms 1 to 6 have extra | hydrogen atoms not depicted. |
The three aromatic | hydrogen atoms of mesitylene are in identical chemical |
iate, resulting from the addition of only two | hydrogen atoms is called dihydroimidazole (imidazoline |
ound formally derived by the addition of four | hydrogen atoms to imidazole. |
Primary amines arise when one of three | hydrogen atoms in ammonia is replaced by an alkyl. |
In tertiary amines, all three | hydrogen atoms are replaced by organic substituents. |
s a cyclic derivate of norleucine, having two | hydrogen atoms less. |
They all contain a carbon frame, and have | hydrogen atoms attached to the frame. |
containing two | hydrogen atoms that can be replaced by metal ions, or |
In a crystalline host the 6 | hydrogen atoms in TMM are identical. |
Aliphatic and aromatic | hydrogen atoms were included implicitly by representin |
phtalenedione) through replacement of all six | hydrogen atoms by hydroxyl (OH) groups. |
oduct of phenol in which one, or more, of the | hydrogen atoms is replaced by iodine. |
ecule causes both methylene groups to contain | hydrogen atoms in exactly the same electronic environm |
entical spectroscopic results provided by the | hydrogen atoms on all methyl groups. |
based on methane, except that two of the four | hydrogen atoms have been replaced by fluorine atoms. |
ists of a 1,4-benzoquinone core with the four | hydrogen atoms replaced by two oxalate groups. |
ganic compound related to ethanol, except the | hydrogen atoms at position 2 are replaced with chlorin |
nsiderably shortened by collisions with other | hydrogen atoms and interaction with the cosmic microwa |
ving from anthraquinone by replacement of two | hydrogen atoms (H) by hydroxyl groups (-OH). |
is a fluorocarbon alkene in which all of the | hydrogen atoms in propylene are replaced by fluorine a |
ecule consists of a benzene core with the six | hydrogen atoms replaced by three oxalate groups. |
phtalenedione) through replacement of all six | hydrogen atoms by hydroxyl (OH) groups. |
with a technetium atom in the center and six | hydrogen atoms at the corners. |
wo chlorine atoms would take the place of two | hydrogen atoms (CHCl2CO2H). |
ither contain hydroxyl groups and/or pairs of | hydrogen atoms that are substituted by oxygen atoms. |
ecule consists of a benzene core with the six | hydrogen atoms replaced by three carbonate groups. |
of naphthalene through the replacement of two | hydrogen atoms by two ketone groups. |
cid radical is an anion left after removal of | hydrogen atoms from an acid, for example NO3- and SO4- |
than strong acids, which release all of their | hydrogen atoms when dissolved in water. |
ists of a 1,4-benzoquinone core with the four | hydrogen atoms replaced by two carbonate groups. |
In this process two | hydrogen atoms generated from NADH and an accompanying |
ts, with the result that all carbon atoms and | hydrogen atoms appear equivalent on the NMR timescale. |
orm positronium atoms which then reacted with | hydrogen atoms from the methane. |
time dealt with determining the positions of | hydrogen atoms in materials. |
the bond joining the rings is limited by the | hydrogen atoms, enantiomerically pure NOBIN may racemi |
thod involves bombarding germanium metal with | hydrogen atoms (H) that are generated using a high fre |
ach other, with each carbon atom having three | hydrogen atoms bonded to it. |
points on its structure capable of supporting | hydrogen atoms not currently part of the structure. |
This paved the way for her discovery that | hydrogen atoms absorbed in the bulk of a nickel sample |
UPAC names, "dihydro" refers to the two added | hydrogen atoms needed to remove one double bond from t |
can be seen as a methane molecule, whose four | hydrogen atoms are each replaced with a different halo |
derived from anthraquinone by replacing three | hydrogen atoms by hydroxyl groups. |
carbon atoms in the chain there is a pair of | hydrogen atoms such that the chemical formula is C11H2 |
anded molecule also exists, although with the | hydrogen atoms replaced by phenyl groups. |
s cubane (C8H8) except that each of the eight | hydrogen atoms is replaced by a nitro group (NO2). |
In contrast, the | hydrogen atoms are all bridging in α-alane, a high-mel |
benzene derivative, is capable of abstracting | hydrogen atoms from the sugar backbone of DNA which re |
his occurs because the two ionization capable | hydrogen atoms on the acid molecule do not leave the a |
Protoporphyrinogen oxidase removes | hydrogen atoms from protoporphyrinogen IX (the product |
there are any) are usually listed first, any | hydrogen atoms are listed next, and all other elements |
heory if not in practice, the fusion of light | hydrogen atoms with heavier atoms such as lithium or b |
cing chlorine atoms in the chloroethenes with | hydrogen atoms via hydrogenolytic reductive dechlorina |
ses to produce the corresponding hydrocarbon ( | hydrogen atoms substitute the original chlorine atoms) |
vative of m-xylene in which the four aromatic | hydrogen atoms are replaced by chlorine. |
ed from anthraquinone by replacement of three | hydrogen atoms by hydroxyl (OH) groups. |
by substituting isopropyl groups for the two | hydrogen atoms attached to the non-aromatic nitrogen a |
rocarbon with the n-butane skeleton, but with | hydrogen atoms in n-butane are replaced with fluorine |
diradical, 1,4-dehydrobenzene, then abstracts | hydrogen atoms from the sugar backbone of DNA, which r |
metric, and the bonding between the metal and | hydrogen atoms is significantly ionic. |
α-eleostearic acid by the replacement of two | hydrogen atoms by two hydroxyl (OH) groups. |
ed from anthraquinone by replacement of three | hydrogen atoms by hydroxyl (OH) groups. |
from anthraquinone by the replacement of two | hydrogen atoms by hydroxyl groups (OH). |
that the bonds between boron and the terminal | hydrogen atoms are conventional 2-center, 2-electron c |
ding between the boron atoms and the bridging | hydrogen atoms is, however, different from that in mol |
used two electrons in bonding to the terminal | hydrogen atoms, each boron has one valence electron re |
In the cis conformation, | hydrogen atoms are on the same side of the double bond |
Free | hydrogen atoms are able to bind to the SiO2 silica gla |
adjacent to them does not contain any bonded | hydrogen atoms with which they can interact. |
r of the molecule, two of which are bonded to | hydrogen atoms and the other two nitrogens forming par |
ing of five carbon atoms each bonded with two | hydrogen atoms above and below the plane. |
anthraquinone through the replacement of six | hydrogen atoms (H) by hydroxyl groups (OH). |
pyrimidine which is the result of adding two | hydrogen atoms to a uridine, making it a fully saturat |
roperties of simple arsole derivatives, where | hydrogen atoms are substituted by other atoms or small |
of naphthoquinone through replacement of two | hydrogen atoms (H) by hydroxyl groups (OH). |
increased (methyl groups are larger than the | hydrogen atoms they replace), reducing the strongest p |
be obtained from adamantane by removal of two | hydrogen atoms to create an internal bond. |
edges meet at each corner, there would be no | hydrogen atoms, thus this hypothetical octahedron mole |
a cyclohexane ring by a formal addition of 6 | hydrogen atoms while the alkyl and ester groups are no |
nique of neutron diffraction that allowed the | hydrogen atoms to be located with greater precision. |
portant reactions, such as the abstraction of | hydrogen atoms from tocopherol and polyunstaturated fa |
1,4-naphthoquinone through replacement of two | hydrogen atoms by hydroxyl (OH) groups. |
m furan C4H4O through replacement of the four | hydrogen atoms by carboxyl functional groups -(CO)OH. |
c orbitals form regular bonds with two of the | hydrogen atoms as in a planar alkene. |
uinone C6H4O2 through replacement of the four | hydrogen atoms by carboxyl functional groups -(CO)OH. |
hat can be seen as the result of removing two | hydrogen atoms from a butane molecule, leaving two fre |
g radiation such as solar UV light, the outer | hydrogen atoms can be stripped off and replaced with a |
xene with four hydroxyl groups (OH) replacing | hydrogen atoms on the four carbon atoms not adjacent t |
their properties by uniting with one to four | hydrogen atoms, in such a manner that the resulting co |
a molecule is indicated first, the number of | hydrogen atoms next, and then the number of all other |
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