Examples of 'addition reactions' in a sentence
Meaning of "addition reactions"
addition reactions - in chemistry, a type of chemical reaction where two or more molecules combine to form a larger molecule
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- plural of addition reaction
How to use "addition reactions" in a sentence
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addition reactions
Addition reactions are very fast and exothermic.
Pericyclic reactions are usually rearrangement or addition reactions.
Various other addition reactions are also known.
There are many variations of nucleophilic addition reactions.
Exemplary addition reactions include the following.
Distinguish between substitution and addition reactions.
Addition reactions of this type are numerous.
Such bonds can undergo addition reactions.
Addition reactions are also encountered in polymerizations and called addition polymerization.
An effective amount of an initiator of thiolene addition reactions.
A series of addition reactions ensues.
Undergoes substitution rather than addition reactions.
Most of these addition reactions follow the mechanism of electrophilic addition.
An esr study of the addition reactions of.
Most addition reactions to alkenes follow the mechanism of electrophilic addition.
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Free radicals may be generated in the thermal addition reactions.
Addition reactions in which two or molecules combine form an important class of compounds.
Nucleophilic addition reactions.
These salts were used for studies of regioselectivity in nucleophilic addition reactions.
Conjugate addition reactions for the controlled delivery of pharmaceutically active compounds.
The rule is useful in predicting the molecular structures of products of addition reactions.
Addition reactions take place when two or more reactants combine to form a single product.
A polymerization reaction that forms polymers via individual independent addition reactions.
Conjugate addition reactions may also be carried out using the catalysts of the invention.
Hexafluorothioacetone is highly reactive to alkenes and dienes combining via addition reactions.
Benzene resists addition reactions because that would involve breaking the delocalization and losing that stability.
These references do not describe or suggest curing the resins by thiolene addition reactions.
Thus, bulk or solution addition reactions are acceptable.
The secondary reactions were identified as Michael addition reactions.
Typical addition reactions are schematically represented as follows,.
Tertiary phosphines are known to catalyze Michael addition reactions.
Addition reactions are inherently atom efficient, so are preferred synthesis pathways.
In this respect, isomerization reactions or addition reactions are particularly efficient.
Addition reactions to carbon-carbon double and triple bonds.
Addition-elimination reactions are addition reactions immediately followed by elimination reactions.
Properties of a, β-unsaturated aldehydes and ketones and the conjugate addition reactions.
These reactions are addition reactions and they generate no by-product.
Examples of suitable reactions are radical polymerisation, condensation reactions and addition reactions.
Nucleophilic addition reactions can also be useful in preparing compounds of formula 5.
These occur between alkenes and electrophiles, often halogens as in halogen addition reactions.
In the art ring-opening addition reactions of glycidoxylated benzophenone to amine compounds are described.
In contrast, a coordinatively saturated complex resists undergoing substitution and oxidative addition reactions.
Polyaddition, unlike chain polymerization, involves addition reactions between species of all degrees of polymerization.
Preferred reactions are condensation reactions and / or Michael addition reactions.
Acid-promoted addition reactions are likewise analogous to those of alkenes, including Markovnikov selectivity.
Benzene undergoes substitution reactions, rather than addition reactions as typical for alkenes.
Electrophilic addition reactions for 1-fluoro-acenaphthylene are also described.
A composition as in claim 1 wherein the initiator of thiolene addition reactions is a free radical photointiator.
Non-eliminating addition reactions are the preferred cross-linking mechanism.
This invention relates to supported metallocene catalyst compositions useful for addition reactions of prochiral a-olefins.
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Examples of using Reactions
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