On this page you'll find 10+ example sentences with Nucleophilic. Discover the meaning, how to use the word correctly in a sentence.
Nucleophilic meaning
of, or relating to a nucleophile
Using Nucleophilic
- The main meaning on this page is: of, or relating to a nucleophile
- In the example corpus, nucleophilic often appears in combinations such as: nucleophilic attack, nucleophilic substitution, nucleophilic addition.
Context around Nucleophilic
- Average sentence length in these examples: 19.5 words
- Position in the sentence: 6 start, 11 middle, 3 end
- Sentence types: 20 statements, 0 questions, 0 exclamations
Corpus analysis for Nucleophilic
- In this selection, "nucleophilic" usually appears in the middle of the sentence. The average example has 19.5 words, and this corpus slice is mostly made up of statements.
- Around the word, 130, general, weakly, addition, abstraction and attack stand out and add context to how "nucleophilic" is used.
- Recognizable usage signals include performs a nucleophilic attack on and aren t nucleophilic in their. That gives this page its own corpus information beyond isolated example sentences.
- By corpus frequency, "nucleophilic" sits close to words such as abbe, abeyance and abp, which helps place it inside the broader word index.
Example types with nucleophilic
The same corpus examples are grouped by length and sentence type, making it easier to see the contexts in which the word appears:
Nucleophilic addition with an organogermanium compound. (6 words)
Organohalogens are also synthesized through the nucleophilic abstraction reaction. (9 words)
Nucleophilic addition reactions Nucleophiles add readily to the carbonyl group. (10 words)
First, the 2'OH of a specific branchpoint nucleotide within the intron, defined during spliceosome assembly, performs a nucleophilic attack on the first nucleotide of the intron at the 5' splice site, forming the lariat intermediate. (36 words)
A monosaccharide can switch from the acyclic (open-chain) form to a cyclic form, through a nucleophilic addition reaction between the carbonyl group and one of the hydroxyls of the same molecule. (32 words)
Catalysis Catalysis is achieved by one of two mechanisms: *Aspartic, glutamic and metallo- proteases activate a water molecule which performs a nucleophilic attack on the peptide bond to hydrolyse it. (30 words)
Example sentences (20)
Joule, p. 130 Nucleophilic substitutions In contrast to benzene, pyridine efficiently supports several nucleophilic substitutions, and is regarded as a good nucleophile ( donor number 33.1).
A monosaccharide can switch from the acyclic (open-chain) form to a cyclic form, through a nucleophilic addition reaction between the carbonyl group and one of the hydroxyls of the same molecule.
Another form of ligand exchange is seen in the nucleophilic abstraction reaction.
Catalysis Catalysis is achieved by one of two mechanisms: *Aspartic, glutamic and metallo- proteases activate a water molecule which performs a nucleophilic attack on the peptide bond to hydrolyse it.
Enols are ambident nucleophiles, but, in general, nucleophilic at the alpha carbon atom.
First, the 2'OH of a specific branchpoint nucleotide within the intron, defined during spliceosome assembly, performs a nucleophilic attack on the first nucleotide of the intron at the 5' splice site, forming the lariat intermediate.
Halogens While the halogens aren't nucleophilic in their diatomic form (i.e. I 2 is not a nucleophile), their anions are good nucleophiles.
However, unlike benzene and its derivatives, pyridine is more prone to nucleophilic substitution and metalation of the ring by strong organometallic bases.
In general, sulfur is very nucleophilic because of its large size, which makes it readily polarizable, and its lone pairs of electrons are readily accessible.
It is thought that a hydroxyl ion bridging the two metal ions takes part in nucleophilic attack on the phosphorus ion.
It provides strong acidity with minimal interference because perchlorate is weakly nucleophilic (explaining the high acidity of HClO 4 ).
Mechanism of cellular toxicity The compound readily eliminates a chloride ion by intramolecular nucleophilic substitution to form a cyclic sulfonium ion.
Nucleophilic Abstraction can be used to separate an alkane from a metal.
Nucleophilic addition reactions Nucleophiles add readily to the carbonyl group.
Nucleophilic addition with an organogermanium compound.
Nucleophilic describes the affinity of a nucleophile to the nuclei.
Nucleophilicity Many schemes attempting to quantify relative nucleophilic strength have been devised.
Nucleophilicity, sometimes referred to as nucleophile strength, refers to a substance's nucleophilic character and is often used to compare the affinity of atoms.
Organic chloride compounds tend to be less reactive in nucleophilic substitution reactions than the corresponding bromide or iodide derivatives, but they tend to be cheaper.
Organohalogens are also synthesized through the nucleophilic abstraction reaction.
Common combinations with nucleophilic
These word pairs occur most frequently in English texts: