reformatsky reaction

JEE Mains 2015 Discussion Forum › Organic Chemistry questions › reformatsky reaction

In reformatsky reaction,

why doesnt the ester get hydrolysed when H+ is added after the nucleophilic addition??

UP 0 DOWN 0 0 2
Post on FacebookPost anonymously?

2 Answers

Pritish Chakraborty ·2010-04-04 02:25:23

"Organozinc compounds are prepared from Î±-halogenesters in the same manner as Grignard Reagents. This reaction is possible due to the stability of esters against organozincs. Due to the very low basicity of zinc enolates, there is hardly any competition from proton transfer, and the scope of carbonyl addition partners is quite broad. In presence of ketones or aldehydes, the organozinc compounds react as the nucleophilic partner in an addition to give Î²-hydroxy esters."

- www.organic-chemistry.org

UP 0 DOWN 0
Post on FacebookPost anonymously?

106

Asish Mahapatra ·2010-04-04 06:58:08

thanks pritish

UP 0 DOWN 0
Post on FacebookPost anonymously?

Your Answer

Basic Integral Calculus Operators Symbols Matrix Cases

√ √ || {} [] () → ~ ^ x x x → → ln log lg lim lim cos sin tan cot arcsin arccos arctan

∫ ∫ ∫ ∫ ∫ ∬ ∬ ∬ ∬ ∬ ∭ ∭ ∭ ∭ ∭ ⨌ ⨌ ⨌ ⨌ ⨌

∑ ∑ ∑ ∑ ∑ ∮ ∮ ∮ ∮ ∮ ∏ ∏ ∏ ∏ ∏ ∐ ∐ ∐ ∐ ∐

+ - × ÷ ± ∓ = ∪ ∩ ≠ ∼ ≈ ∅ ∀ ∃ ∈ ∋ ∝ ≤ ≥ ≃ ≅ ≡ < > ≪ ≫ ⊂ ∉ ⊃ ⊆ ⊇ ⇒ ⇐ ⇔ ⇒ ⇐ ⇔ ⇑ ⇓ ⇕ → ← ↔ → ← ↔ ↑ ↓ ↕ ↖ ↗ ↘ ↙ ↪ ↩ ⇀ ↼ ⇁ ↽

° ∂ ∞ α β γ δ θ λ μ ν ξ π ρ σ φ ω ε ƒ κ τ υ Γ Δ Λ Σ Π Ω

Close [X]

reformatsky reaction

2 Answers

Your Answer

Add Image

Similar Questions