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Bonds with hydrogen

Element Electronegativity Covalent radius, pm Usual coordination number Bond with hydrogen Bond length, pm Bond energy, kj/mot ... [Pg.26]

When two sp-hybridized carbon atoms approach each other, sp hybrid orbitals on each carbon overlap head-on to form a strong sp-sp a bond. In addition, the pz orbitals from each carbon form a pz-pz it bond by sideways overlap and the py orbitals overlap similarly to form a py-py tt bond. The net effect is the sharing of six electrons and formation of a carbon-carbon triple bond. The two remaining sp hybrid orbitals each form a acetylene molecule (Figure 1.16). [Pg.18]

Here is a situation we haven t met before. After using the two available partially filled orbitals to form covalent bonds with hydrogen atoms, there remains a vacant valence orbital. In the electron dot formulation (36) we see that the carbon atom finds itself near only six electrons in CH2. The valence orbitals will accommodate eight electrons. Because one valence or-... [Pg.284]

Remember from Chapter H that the hydrogen atoms of water molecules form hydrogen bonds with electronegative O and N atoms, whereas the oxygen atom of a water molecule forms hydrogen bonds with hydrogen atoms in highly polar N—H and O—H bonds. [Pg.951]

Bonding of this type and other boron hydrides that have three-center two-electron bonds with hydrogen bridges is discussed in Chapter 13. [Pg.126]

In some cases, elements having electronegativities too low to give ionic bonding with hydrogen also tend to be unreactive, so that direct combination of the elements is not feasible. In such cases, the procedure just described can be used to prepare the hydride. For example, silicon hydride, SiH4 (known as silane), can be produced by the reactions... [Pg.420]

One of the results of this variety in hydrogen-defect reaction pathways is that it largely clouds one of the hopes of the hydrogenation experiments, namely that the susceptibility of deactivation could provide information on the defect microstructure and the nature of the bonding with hydrogen. [Pg.101]

Gases such as helium, neon and argon are so unreactive that we call them the inert gases. They form no chemical compounds, and their only interactions are of the London dispersion force type. They cannot form hydrogen bonds, since they are not able to bond with hydrogen and are not electronegative. [Pg.74]

As a result of this hybridization, carbon forms four bonds with hydrogen to form the CH4 molecule. [Pg.31]

Explain the hybridization undergone by the boron atom when it bonds with hydrogen. [Pg.45]

An incorrect statement to the effect that there is no evidence for the complexing of double bonds with hydrogen halides must be corrected. This writer himself has quoted several times the demonstration by O. Maas and his collaborators that the HX (X = Cl, Br) do form complexes with alkenes [A, B],... [Pg.236]

Each carbon forms Ncc bonds with other carbon atoms and 4 Nqc bonds with hydrogen atoms. The part of au qk due to that C atom is Ncc cc qc + (4 ATcc)flCHAge- On the other hand, each H atom contributes flHcAgH- Summation over all C and H atoms gives... [Pg.129]

The oct- prefix here tells you that this alkane is eight carbons long. Draw eight linked carbons and fill in the empty bonds with hydrogen. Your structure should look like one of these ... [Pg.99]

Hydrocarbons with one or more carbon-to-carbon double bonds are called alkenes. The names of alkenes end with -ene. Ethene, or ethylene, the simplest alkene, has two carbon atoms connected by a double bond. The double bond consists of two pairs of shared electrons, one pair from one carbon atom and one pair from the other carbon atom. Each of the carbons also has two single bonds with hydrogen atoms so that the formula for the compound can be written as... [Pg.26]

Nitroaminocompounds of the type (II) were also examined in suspension in paraffin oil. They contain NH groups which give rise to bands with frequencies 3030 and 1610 cm1. The r correspond to NH groups bonded with hydrogen bonds. The frequencies of the nitro group are lowered in all nitro niino compounds with an exception of the compound (IIa) which does not contain hydroxyl groups. This may be accounted for by the weakness of bifurcated hydrogen bonds. [Pg.146]

The Third-Group Elements.—The B—F bond has about 63 percent ionic character, B—O 44 percent, B—Cl 22 percent, and so forth. Bor,on forms normal covalent bonds with hydrogen. The aluminum bonds are similar to those of beryllium in ionic character. [Pg.102]


See other pages where Bonds with hydrogen is mentioned: [Pg.168]    [Pg.66]    [Pg.455]    [Pg.187]    [Pg.798]    [Pg.242]    [Pg.22]    [Pg.35]    [Pg.836]    [Pg.225]    [Pg.119]    [Pg.102]    [Pg.66]    [Pg.526]    [Pg.424]    [Pg.24]    [Pg.173]    [Pg.529]    [Pg.31]    [Pg.51]    [Pg.122]    [Pg.80]    [Pg.81]    [Pg.158]    [Pg.12]    [Pg.22]    [Pg.693]    [Pg.37]    [Pg.13]    [Pg.34]    [Pg.308]    [Pg.87]    [Pg.68]    [Pg.36]   
See also in sourсe #XX -- [ Pg.172 ]




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4- Chlorophenol, hydrogen bonding, with

Acids and Amides with Attached Hydrogen-Bonding Groups

Antimony—hydrogen bonds reactions with

Arsenic—hydrogen bonds reactions with

Block Copolymer Systems with Hydrogen-Bonding Interaction in Solution

Boron—carbon bonds reactions with hydrogen

Carbon monoxide with hydrogen-bonding acceptors

Carbon-hydrogen bonds radical reaction with

Carbon—hydrogen bonds reactions with

Carboxylic acids, hydrogen bonding with fluoride

Catalysis Uncoupling with Hydrogen Peroxide Production or Dioxygen Bond Scission

Catalysts with boron—hydrogen bonds

Catalysts with nitrogen—hydrogen bond

Catalysts with phosphorus—hydrogen bond

Catalysts with silicon—hydrogen bond

Cooperative and Anticooperative Energy Effects in Systems with Classical Hydrogen Bonds

Crystal engineering with hydrogen bonds

Dimethylsulfoxide, hydrogen bonding, with

Direct dyes hydrogen bonds with cellulose

Germanium—hydrogen bonds reactions with

Hydrogen Bonding with Other Noncovalent Interactions

Hydrogen Bonds with Varying Strengths

Hydrogen Interaction with Silicon Dangling Bonds

Hydrogen bond acidic polycarbosilanes with

Hydrogen bond fuel cell with

Hydrogen bond lengths with other elements

Hydrogen bond with amino acids

Hydrogen bonding amines with water

Hydrogen bonding carbonyl group with water

Hydrogen bonding steric interference with

Hydrogen bonding systems with strong symmetric bonds

Hydrogen bonding water with amorphous polymer

Hydrogen bonding with oxygen

Hydrogen bonding with peroxy radicals

Hydrogen bonding with polyaniline

Hydrogen bonds with participation

Hydrogen bonds, contact with polar surfaces

Hydrogen bonds, contact with polar surfaces through

Hydrogen covalent bond with

Hydrogen, bonding with carbon

Hydrogen-Bonded Complexes with Polar Organic Compounds

Hydrogen-Bonded Networks Constructed with 5-Nitrobarbiturate

Hydrogen-bond acceptors interactions with donors

Hydrogen-oxygen bonds reactions with

Hydrogenation of Compounds with CC Bonds

Hydrogenation of Multiple Bonds with Metal Nanoparticles in Ionic Liquids

Hydrogenation, catalytic bond isomerization with alkenes

Hydrogenation, catalytic bond migration with alkenes

Ice and Other Structures with Disordered Hydrogen Bonds

Infrared absorptions associated with hydrogen bonding

Insertion reactions with carbon-hydrogen bonds

Iodine, interactions with hydrogen-bond

Nano-Morphology Formation in Polymer Blends without and with Hydrogen Bonding

Nitrogen—hydrogen bonds reactions with

Phenols hydrogen bonding with solvent

Phosphorus—hydrogen bonds reactions with

Polymers Connected with Bivalent Hydrogen Bonds

Polymers Connected with Multiple Hydrogen Bonds

Polymers Connected with Quadruple Hydrogen Bonds

Polymers Connected with Trivalent Hydrogen Bonds

Polymers with Hydrogen-Bonding Motifs

Polymers with hydrogen bond chains

Problems Associated with the Hydrogen-Bond Geometry

Proton Transfer in Systems with the Intramolecular Hydrogen Bonding

Reaction with Free Radicals Hydrogen Atom Abstraction and One- or Three-Electron Bonding

Self-assembly with hydrogen bonding

Self-assembly with hydrogen bonding polymers

Silicon—hydrogen bonds reactions with

Sulfur—hydrogen bonds reactions with

Trimethylamine, hydrogen-bonded with

Trimethylamine, hydrogen-bonded with water

With phosphorus-hydrogen bonds

With silicon-hydrogen bonds

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