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Hydrogen atoms, bond formation

Trimethylamine replaces PH3 quantitatively in BH3 PH3 to give BH3 N(CH3)3. Liquid or gaseous ammonia also replaces phosphine in the compound BH3 PH3 to the extent of 52-58% or up to 75%, respectively. The hydrogen atoms bonded to boron are partially, or completely, replaced by chlorine on treatment with hydrogen chloride, depending on the reaction conditions. The first stage of the reaction with hydrogen chloride is the formation of the colourless, viscous liquid BHjCl PH3 (see below). [Pg.34]

In the preparation of polyethylene, ethene molecules (C2H4) are bonded together to form a long carbon chain, with two hydrogen atoms bonded to each internal carbon atom and three hydrogen atoms bonded to the end carbon atoms. Draw polyethylene and explain why the formation of polyethylene is an addition reaction. [Pg.223]

The formation of single, double, and triple bonds in a molecule depends upon the types of hybridized orbitals that are sharing electrons. For example, when two hydrogen atoms bond to form H2(g), there is an overlap of s orbitals as shown in Figure 5.13. [Pg.88]

The amino group comes from ammonia. All of the carbon atoms are derived from methane. The hydrogen atoms bonded to the carbon atoms remain with the methane during bond formation or they may come from hydrogen gas. The oxygen atoms of the carboxyl group are from water. [Pg.1452]

The functional group of esters, —C—O—, is bonded to two alkyl groups, except for formates, which have a hydrogen atom bonded to the carbon atom of the functional group. [Pg.154]

The scope of the ene reaction has been extended by the discovery that allylic metal reagents (e.g. metals Mg, Zn, Li, Ni, Pd, Pt) take part readily by migration of the metal atom (instead of a hydrogen atom) and formation of a new carbon-metal bond. For example, addition of crotyl magnesium chloride to trimethylsilylethene... [Pg.235]

It is possible to associate the small yield of monomer with the fact that most C-C bonds scissions are accompanied by the transfer of hydrogen atoms. The formation of monomer is possible via cleavage of the carbon-carbon bonds located at the P-position relative to the double bond, which are the weakest, without transfer of a hydrogen atom ... [Pg.51]

When two hydrogen atoms are relatively far apart their total energy is simply that of two isolated hydrogen atoms (I). Formation of a covalent bond reduces the overall energy... [Pg.23]

In contrast to the (100) surface, hydrogen termination of the surface danghng bonds stabihzes the diamond (111) surface in its bulk-terminated form as shown in Figtu-e 10.12a without any notable deviation of the carbon atoms from their respective bulk positions. Instead of carrying a danghng bond, each surface atom is passivated by a hydrogen atom. The formation of the covalent carbon-hydrogen... [Pg.446]


See other pages where Hydrogen atoms, bond formation is mentioned: [Pg.95]    [Pg.5]    [Pg.166]    [Pg.7]    [Pg.95]    [Pg.260]    [Pg.422]    [Pg.86]    [Pg.207]    [Pg.105]    [Pg.170]    [Pg.422]    [Pg.115]    [Pg.331]    [Pg.98]    [Pg.229]    [Pg.170]    [Pg.541]    [Pg.117]    [Pg.300]    [Pg.541]    [Pg.29]    [Pg.224]    [Pg.30]    [Pg.317]    [Pg.250]    [Pg.308]    [Pg.313]    [Pg.386]    [Pg.20]    [Pg.213]    [Pg.23]    [Pg.747]    [Pg.188]    [Pg.197]    [Pg.703]    [Pg.713]    [Pg.436]    [Pg.141]    [Pg.143]    [Pg.324]   


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Atom bonding

Atomic bonding

Atoms bonds

Atoms, formation

Bonds atomic

Formation hydrogen bonding

Hydrogen atom formation

Hydrogen bond formation

Hydrogen bonding atoms

Hydrogen formation

Hydrogenation formation

Hydrogenations formate

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