Examples of using C-h in English and their translations into Indonesian
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Ecclesiastic
NaHMDS is widely used as a base for C-H acids.
Because of this property, C-H bonds alpha(adjacent) to the nitro group can be acidic.
Also, nearly all organic compounds contain carbon-hydrogen or C-H bonds.
Very strong bases can deprotonate weak acidic C-H groups even in the absence of water.
A harmonic oscillator in classical mechanics(A-B) and quantum mechanics(C-H).
People also translate
In the methane molecule(CH4) the four C-H bonds are arranged tetrahedrally around the carbon atom.
In the case of polyesters, there is dipole-dipole bonding between the oxygen atoms in C=O groups andthe hydrogen atoms in C-H groups.
This large kinetic isotope effect shows that the C-H(or C-D) bond breaks in the rate-determining step.
The relative rates of the chlorination is partially explained by the differing bond dissociation energies,425 and 411 kJ/mol for the two types of C-H bonds.
Each contains a benzene ring in which two of the C-H fragments have been replaced by isolobal nitrogen.
If the spectrum has a characteristic peak in the range of 4,000 to 2,500,the peak corresponds to absorption caused by N-H, C-H and O-H single bonds.
Each carbon atom has four bonds(either C-H or C-C bonds), and each hydrogen atom is joined to a carbon atom(H-C bonds).
The carbon-fluorine bond is very strong(stronger than C-H) and isn't easily broken.
Each carbon atom must have 4 bonds(either C-H or C-C bonds), and each hydrogen atom must be joined to a carbon atom(H-C bonds).
Very strong bases are evenable to deprotonate very weakly acidic C-H groups in the absence of water.
Metal-catalyzed C-H Borylation reactions are transition metal catalyzed organic reactions that produce an organoboron compound through functionalization of aliphatic and aromatic C-H bonds.
Inorganic chemistry covers all materials that aren't organic and are termed as nonliving substances-the compounds that do not comprise a carbon-hydrogen(c-h) bond.
This field covers all chemicalcompounds except the myriad organic compounds(compounds containing C-H bonds), which are the subjects of organic chemistry.
Stability of carbocations:(CH3)3C+gt;(CH3)2CH+gt;(CH3)CH2+gt; CH3+ The three C-H σ bonds of the methyl group(s) attached to the carbocation can undergo the stabilization interaction but only one of them can be aligned perfectly with the empty p-orbital, depending on the conformation of the carbon-carbon bond.
Since not all carbon reactions are organic, another way to understand organic chemistry wouldbe to study the molecules containing carbon-hydrogen(C-H) bond and their reactions.
For example, in diatomic nitrogen N≡N the bond order is 3,in acetylene H-C≡C-H the bond order between the two carbon atoms is also 3, and the C-H bond order is 1.
Since not all carbon reactions are organic, another way to look at organic chemistry would be toconsider it the study of molecules containing the carbon-hydrogen(C-H) bond and their reactions.
The CFCs are far less flammable than methane,in part because they contain fewer C-H bonds and in part because, in the case of the chlorides and bromides, the released halides quench the free radicals that sustain flames.
One notes that correct alignment of the sample rotation axis as close as possible to θm is essential for cancelling out the dipolar interactions whose strength for angles sufficiently far from θmis usually greater than~10 kHz for C-H bonds in solids, for example, and it is thus greater than their CSA values.