Advertisements
Advertisements
प्रश्न
Can we use nucleophiles such as NH3, CH3O for the Nucleophilic substitution of alcohols?
Advertisements
उत्तर
1. Increasing order of nucleophilicity,
NH3 < –OH⊕ < CH3O⊖
2. Higher electron density will increase nucleophilicity.
3. Negatively charged species are almost always more nucleophiles than neutral species.
4. RO⊖ has an alkyl group attached, allowing a greater amount of polarizability. This means oxygen’s lone pairs will be more readily available to reach in RO⊖ than in OH⊖. Hence CH3O– is the better nucleophile for the nucleophilic substitution of alcohols. NH3 cannot act as a nucleophile for the nucleophilic substitution of alcohols.
APPEARS IN
संबंधित प्रश्न
Which of the following compounds on reaction with methyl magnesium bromide will give tertiary alcohol.
Draw the major product formed when 1-ethoxyprop-1-ene is heated with one equivalent of HI.
Write the mechanism of acid catalysed dehydration of ethanol to give ethene.
Complete the following reaction.
\[\ce{C6H5 - OH ->[Zn dust] A ->[CH3Cl][Anhydrous AlCl3] B ->[acid KMnO4] C}\]
Phenol is distilled with Zn dust followed by Friedel-crafts alkylation with propyl chloride to give a compound B, B on oxidation gives (c) Identify A, B and C.
What will be the product (X and A) for the following reaction?
\[\ce{acetylchloride ->[i) CH3MgBr][ii) H3O^+] X ->[acid K2Cr2O7] A}\]
How will you convert acetylene into n-butyl alcohol?
What will be the product (X and A) for the following reaction:
\[\ce{acetylchloride ->[i) CH3MgBr][ii) H3O+]X->[acid K2Cr2O7]A}\]
Draw the major product formed when 1-ethoxyprop-1-ene is heated with one equivalent of HI.
What will be the product (X and A)for the following reaction
\[\ce{acetylchloride ->[i) CH3MgBr][ii) H3O^+]X ->[acid K2Cr2O7]A}\]
