So, is ethanol a strong nucleophile? Is ethanol a strong nucleophile? To answer this question, first, we can take a look at the acidity and alkalinity of ethanol. Strictly speaking, it cannot cause the acid-base indicator to change color, nor can it react chemically with alkali. Therefore,...
Ask a question Search AnswersLearn more about this topic: Nucleophile | Definition, Reactions & Examples from Chapter 4 / Lesson 18 36K Learn about nucleophiles, what makes a strong nucleophile, and the nucleophilicity trend. See common nucleophiles examples and their role in che...
Which of the following is considered a strong base? a. NH3 b. Be(OH)2 c. Mg(OH)2 d. Ba(OH)2 Consider these three anions. 1. Which one is the strongest base? 2. Which one the weakest base? 3. Which one is the nucleophile? What is the stronger base, OH^- or ...
In another type of reaction, CH-acidic compounds in the presence of a strong base react with aldonitrones by CC bond formation to form a hydroxylamine. Formed from the reaction of (78) and dimethyl malonate, the adduct (81) undergoes cyclization to an azlactone 〈71LA(748)143〉. Sign in...
diatomic anion with chemical formula OH−. It consists of an oxygen and hydrogen atom held together by a single covalent bond, and carries a negative electric charge. It is an important but usually minor constituent of water. It functions as a base, a ligand, a nucleophile, and a ...
The putative active site of yDdi1 RVP is similar to that of HIV-1 protease, including a water molecule that could act as a nucleophile for peptide bond hydrolysis. The first direct evidence that Ddi1-like RVP can act as a protease was presented by Perteguer and coworkers, who showed ...
In the absence of their acid/base residue, thioglycoligases require both an activated glycosyl donor to form the glycosyl-enzyme intermediate and an acceptor that is a strong nucleophile, capable of reacting without basic catalytic assistance (Fig. 1a); consequently, nucleophiles successfully assayed ...
Cyclohexylamine (C6H13N) reacts with benzoyl chloride (C7H5ClO) in a reaction with 1 M NaCO3 acting as the strong base. What is the major product and what is its name? Draw the SN1 mechanism for the reaction of (CH_3CH_2)_3C-Br with chloride ion. ...
A good nucleophile is a good Lewis base. This means that it is able to donate an electron pair. The factor that we can...See full answer below.Become a member and unlock all Study Answers Start today. Try it now Create an account Ask a question Our experts can an...
thereof, y is a positive integer equal to at least 1, subject to the proviso that (a) at least three carbon atoms separate any amino (--NH2) group from any other amino (--NH2) group, and (b) at least two carbon atoms separate any amino group (--NH2) from any other nucleophile....