Search results
Results From The WOW.Com Content Network
Expressing resonance when drawing Lewis structures may be done either by drawing each of the possible resonance forms and placing double-headed arrows between them or by using dashed lines to represent the partial bonds (although the latter is a good representation of the resonance hybrid which is not, formally speaking, a Lewis structure).
A Lewis base, then, is any species that has a filled orbital containing an electron pair which is not involved in bonding but may form a dative bond with a Lewis acid to form a Lewis adduct. For example, NH 3 is a Lewis base, because it can donate its lone pair of electrons.
Unlike other chemical formula types, [a] which have a limited number of symbols and are capable of only limited descriptive power, structural formulas provide a more complete geometric representation of the molecular structure. For example, many chemical compounds exist in different isomeric forms, which have different enantiomeric structures ...
They can form a chemical bond between two atoms, or they can occur as a lone pair of valence electrons. They also fill the core levels of an atom. Because the spins are paired, the magnetic moment of the electrons cancel one another, and the pair's contribution to magnetic properties is generally diamagnetic .
Orbitals of same symmetry and similar energy levels can then be mixed to form a new set of molecular orbitals with bonding, nonbonding, and antibonding characteristics. In the simple MO diagram of H 2 O , the 2s orbital of oxygen is mixed with the premixed hydrogen orbitals, forming a new bonding (2 a 1 ) and antibonding orbital (4 a 1 ).
Diazo compounds have two main Lewis structures in resonance: R 2 >C − –N + ≡N and R 2 >CH=N + =N −. In organic chemistry, the diazo group is an organic moiety consisting of two linked nitrogen atoms at the terminal position.
A frustrated Lewis pair (FLP) is a compound or mixture containing a Lewis acid and a Lewis base that, because of steric hindrance, cannot combine to form a classical adduct. [1] Many kinds of FLPs have been devised, and many simple substrates exhibit activation.
The Simplified Molecular Input Line Entry System (SMILES) is a specification in the form of a line notation for describing the structure of chemical species using short ASCII strings. SMILES strings can be imported by most molecule editors for conversion back into two-dimensional drawings or three-dimensional models of the molecules.