The Schiff base is an example of a nucleophile.
True
False
A Schiff base (named after Hugo Schiff) is a compound with the general structure R2C=NR' (R' ≠ H).They can be considered a sub-class of imines, being either secondary ketimines or secondary aldimines depending on their structure. The term is often synonymous with azomethine which refers specifically to secondary aldimines (i.e. R-CH=NR' where R' ≠ H).
These Schiff base acts as Electrophile not as nucleophile because of the presence of electrophilic center at Sp2 carbon as shown below-
Amines can act as 1 point O Nucleophiles Bronsted Bases Both as Nucleophile and Bronsted base O Neither as Nucleophile nor Bronsted base Clear selection Amides + LiALH4 = amines 1 point True False Imines + NaBH4 = amines 1 point true false amides + Br2 in NaOH = amines 1 point true
4. The Schiff base complex (XX) showed excellent photophysical properties and scientists found applications in fluorescent microscopy imaging of living cells. [Ref: Yang Hai and coworkers, Chemical Communications 2011, 47, 2435-2437. DOI: 10.1039/c0cc04113k]. Suggest a synthetic scheme for the Schiff base complex (XX). Each building block should contain less than 9 carbon atoms. (6 points)
4. The Schiff base complex (XX) showed excellent photophysical properties and scientists found applications in fluorescent microscopy imaging of living cells. [Ref: Yang Hai and...
what is the mechanism of the synthesis of schiff base ligand. using ortho vanaline and L alanine.
strong nucleophile weak base strong bulky base strong nucleophile strong base Promote SN2/E2 weak nucleophile weak base Promote SN1/E1 Promote SN2 Promote E2 CH Br HS NCT HO CHO CHÚCHO NaNO NaOH NOME Noe HOORS Conjugate acids have pka 16-18 Conjugate acids Recall, you make hydroxide have pka 11 or alkoxide ons from the corresponding alcohol or water and Nat CH,OH (MOH) HO CH,CH,OH (EXOH) | HC-Ć-o to CH tert-BUOK NOCH KOHBU NEOBU The structures above are all ways of...
Schiff-base linkage is found in all of the following enzyme, EXCEPT Group of answer choices Transaldolase aldolase glycogen phosphorylase pyruvate carboxylase none of the above
Draw the structure of a Schiff base between pyridoxal-5’-phosphate (PLP) and the epsilon (E) amino group of lysine of an enzyme.
11) Indicate whether the statement about nucleophilicity is or True or False: a) A species with a negative charge is a stronger nucleophile than a similar neutral species. (True / False) b) In particular, a base is a stronger nucleophile than its conjugate acid. (True / False) c) Nucleophilicity decreases from left to right in the periodic table, following the increase in electronegativity from left to right. (True / False) d) The more electronegative elements have more tightly held nonbonding electrons...
What charge would the Schiff-base H2salpn (salicylaldehyde and 1,3-diaminopropane) take if it was to coordinate with [MnIII(AcAc)3]?
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Amines can act as 1 point Nucleophiles Bronsted Bases Both as Nucleophile and Bronsted base Neither as Nucleophile nor Bronsted base Amides + LiALH4 = amines * 1 point O True O False Imines + NaBH4 = amines 1 point true O false amides + Br2 in NaOH = amines 1 point O true O False
7&8 please
7. True or False: Iodide is the best nucleophile in polar protic and polar aprotic solvents. 8. Select the alkyl halide that would be expected to undergo the fastest E2 reaction. or yor yor