「HYDROGEN」の共起表現(1語右が「atoms」) - Weblio英語共起表現検索


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Weblio 辞書 > 英和辞典・和英辞典 > HYDROGENの意味・解説 > HYDROGENに関連した共起表現

「HYDROGEN」の共起表現一覧(1語右が「atoms」)

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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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