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Steric hindrance is a consequence of steric effects. Steric hindrance is the slowing of chemical reactions due to steric bulk. It is usually manifested in intermolecular reactions, whereas discussion of steric effects often focus on intramolecular interactions. Steric hindrance is often exploited to control selectivity, such as slowing unwanted ...
The protonation of substituted aniline is inhibited by steric hindrance. When protonated, the nitrogen in the amino group changes its orbital hybridization from sp 2 to sp 3 , becoming non-planar. This leads to steric hindrance between the ortho-substituted group and the hydrogen atom of the amino group, reducing the stability of the conjugate ...
Adding "steric hindrance" to a molecule's reactive site through bulky groups is a common strategy in molecular chemistry to stabilize reactive moieties within a molecule. [3] In this case bulky ligands like terphenyls , bulky alkoxides , aryl-substituted NHCs , etc. serve as a protective wrapper on the molecule. [ 1 ]
While relationships between thermodynamic stability and kinetic persistency is highly case-dependent, organic radicals can be generally stabilized by any or all of these factors: the presence of electronegativity, delocalization, and steric hindrance. [8] The compound 2,2,6,6-tetramethylpiperidinyloxyl illustrates the combination of all three ...
On the molecular level, the interlocked molecules cannot be separated without the breaking of the covalent bonds that comprise the conjoined molecules; this is referred to as a mechanical bond. Examples of mechanically interlocked molecular architectures include catenanes , rotaxanes , molecular knots , and molecular Borromean rings .
Since the conditions of the reaction are rather forcing, protecting groups are often used to pacify other parts of the reacting molecules (e.g. other alcohols, amines, etc.) The Williamson ether synthesis is a common organic reaction in industrial synthesis and in undergraduate teaching laboratories.
The stereoelectronic effect, which is the interaction shown above when the acceptor orbital is the σ*(Si–CH 3), appears to be a more predominant factor in determining the reaction selectivity against the steric hindrance and even wins over the penalty of the disrupted conjugation system of the product due to steric clash. [23]
steric hindrance around the α-carbon increases. a stronger base is used. temperature increases (increase entropy) the base is a poor nucleophile. Bases with steric bulk, (such as in potassium tert-butoxide), are often poor nucleophiles.