Can you explain the answer of this question below:Which of the followi...
Carbon is less electronegative than nitrogen, so in CH3- all the electron density will be on the carbon. It will be VERY interested in removing its negative charge, i.e., it will be looking for a proton or other cation. Recall that although NH2- is a very bad leaving group, it still is a leaving group, which shows it can exist. To my knowledge, you will never find CH3- as a leaving group. That's one reason alkanes are essentially nonreactive.
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Can you explain the answer of this question below:Which of the followi...
Explanation:
A nucleophile is an atom or molecule that donates a pair of electrons to form a chemical bond with another atom or molecule. The strength of a nucleophile depends on its ability to donate electron density. The stronger the nucleophile, the more likely it is to donate electrons.
Comparison of the answer choices:
A. C2H5SH: This is a weak nucleophile because the S atom is not very electronegative and has a relatively low electron density.
B. CH3COO-: This is the strongest nucleophile because the O atom is highly electronegative and has a high electron density. Additionally, the negative charge on the ion increases the electron density even further.
C. CH3NH2: This is a moderate nucleophile because the N atom is moderately electronegative and has a moderate electron density.
D. NC-CH2: This is a moderate nucleophile because the N atom is moderately electronegative and has a moderate electron density.
Conclusion:
Based on the comparison of the answer choices, we can conclude that the strongest nucleophile is CH3COO-.
Can you explain the answer of this question below:Which of the followi...
Ys.. B is correct opt.. as a nucleophile with a -ve charge is stronger than the neutral...
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