Complete the following reaction :HC ≡ CH H 2SO 4→Hg 2+(A) →O(B).
HC≡C−H
HC≡C−H
HC≡C−H
HC≡C−H H
HC≡C−H H 2
HC≡C−H H 2
HC≡C−H H 2 SO
HC≡C−H H 2 SO 4
HC≡C−H H 2 SO 4
HC≡C−H H 2 SO 4
HC≡C−H H 2 SO 4 →
HC≡C−H H 2 SO 4 →
HC≡C−H H 2 SO 4 →
HC≡C−H H 2 SO 4 → Hg
HC≡C−H H 2 SO 4 → Hg 2+
HC≡C−H H 2 SO 4 → Hg 2+
HC≡C−H H 2 SO 4 → Hg 2+
HC≡C−H H 2 SO 4 → Hg 2+
HC≡C−H H 2 SO 4 → Hg 2+ Acetaldehdye (A)
HC≡C−H H 2 SO 4 → Hg 2+ Acetaldehdye (A) CH
HC≡C−H H 2 SO 4 → Hg 2+ Acetaldehdye (A) CH 3
HC≡C−H H 2 SO 4 → Hg 2+ Acetaldehdye (A) CH 3
HC≡C−H H 2 SO 4 → Hg 2+ Acetaldehdye (A) CH 3 −
HC≡C−H H 2 SO 4 → Hg 2+ Acetaldehdye (A) CH 3 − O
HC≡C−H H 2 SO 4 → Hg 2+ Acetaldehdye (A) CH 3 − O ∣∣
HC≡C−H H 2 SO 4 → Hg 2+ Acetaldehdye (A) CH 3 − O ∣∣
HC≡C−H H 2 SO 4 → Hg 2+ Acetaldehdye (A) CH 3 − O ∣∣
HC≡C−H H 2 SO 4 → Hg 2+ Acetaldehdye (A) CH 3 − O ∣∣ C
HC≡C−H H 2 SO 4 → Hg 2+ Acetaldehdye (A) CH 3 − O ∣∣ C
HC≡C−H H 2 SO 4 → Hg 2+ Acetaldehdye (A) CH 3 − O ∣∣ C −H
HC≡C−H H 2 SO 4 → Hg 2+ Acetaldehdye (A) CH 3 − O ∣∣ C −H
HC≡C−H H 2 SO 4 → Hg 2+ Acetaldehdye (A) CH 3 − O ∣∣ C −H
HC≡C−H H 2 SO 4 → Hg 2+ Acetaldehdye (A) CH 3 − O ∣∣ C −H [O]
HC≡C−H H 2 SO 4 → Hg 2+ Acetaldehdye (A) CH 3 − O ∣∣ C −H [O]oxidation
HC≡C−H H 2 SO 4 → Hg 2+ Acetaldehdye (A) CH 3 − O ∣∣ C −H [O]oxidation
HC≡C−H H 2 SO 4 → Hg 2+ Acetaldehdye (A) CH 3 − O ∣∣ C −H [O]oxidation
HC≡C−H H 2 SO 4 → Hg 2+ Acetaldehdye (A) CH 3 − O ∣∣ C −H [O]oxidation Acetic acid (B)
HC≡C−H H 2 SO 4 → Hg 2+ Acetaldehdye (A) CH 3 − O ∣∣ C −H [O]oxidation Acetic acid (B) CH
HC≡C−H H 2 SO 4 → Hg 2+ Acetaldehdye (A) CH 3 − O ∣∣ C −H [O]oxidation Acetic acid (B) CH 3
HC≡C−H H 2 SO 4 → Hg 2+ Acetaldehdye (A) CH 3 − O ∣∣ C −H [O]oxidation Acetic acid (B) CH 3
HC≡C−H H 2 SO 4 → Hg 2+ Acetaldehdye (A) CH 3 − O ∣∣ C −H [O]oxidation Acetic acid (B) CH 3 −
HC≡C−H H 2 SO 4 → Hg 2+ Acetaldehdye (A) CH 3 − O ∣∣ C −H [O]oxidation Acetic acid (B) CH 3 − O
HC≡C−H H 2 SO 4 → Hg 2+ Acetaldehdye (A) CH 3 − O ∣∣ C −H [O]oxidation Acetic acid (B) CH 3 − O ∣∣
HC≡C−H H 2 SO 4 → Hg 2+ Acetaldehdye (A) CH 3 − O ∣∣ C −H [O]oxidation Acetic acid (B) CH 3 − O ∣∣
HC≡C−H H 2 SO 4 → Hg 2+ Acetaldehdye (A) CH 3 − O ∣∣ C −H [O]oxidation Acetic acid (B) CH 3 − O ∣∣
HC≡C−H H 2 SO 4 → Hg 2+ Acetaldehdye (A) CH 3 − O ∣∣ C −H [O]oxidation Acetic acid (B) CH 3 − O ∣∣ C
HC≡C−H H 2 SO 4 → Hg 2+ Acetaldehdye (A) CH 3 − O ∣∣ C −H [O]oxidation Acetic acid (B) CH 3 − O ∣∣ C
HC≡C−H H 2 SO 4 → Hg 2+ Acetaldehdye (A) CH 3 − O ∣∣ C −H [O]oxidation Acetic acid (B) CH 3 − O ∣∣ C −OH
HC≡C−H H 2 SO 4 → Hg 2+ Acetaldehdye (A) CH 3 − O ∣∣ C −H [O]oxidation Acetic acid (B) CH 3 − O ∣∣ C −OH
HC≡C−H H 2 SO 4 → Hg 2+ Acetaldehdye (A) CH 3 − O ∣∣ C −H [O]oxidation Acetic acid (B) CH 3 − O ∣∣ C −OH .
HC≡C−H H 2 SO 4 → Hg 2+ Acetaldehdye (A) CH 3 − O ∣∣ C −H [O]oxidation Acetic acid (B) CH 3 − O ∣∣ C −OH .Hydration of acetylene (followed by keto enol tautomerism) gives acetaldehdye. This is followed by oxidation to form acetic acid.
Answers & Comments
Answer:
Hence it is named 3-Methylheptane.
Explanation:
Explanation:
Complete the following reaction :
Complete the following reaction :HC ≡ CH H 2SO 4→Hg 2+(A) →O(B).
HC≡C−H
HC≡C−H
HC≡C−H
HC≡C−H H
HC≡C−H H 2
HC≡C−H H 2
HC≡C−H H 2 SO
HC≡C−H H 2 SO 4
HC≡C−H H 2 SO 4
HC≡C−H H 2 SO 4
HC≡C−H H 2 SO 4 →
HC≡C−H H 2 SO 4 →
HC≡C−H H 2 SO 4 →
HC≡C−H H 2 SO 4 → Hg
HC≡C−H H 2 SO 4 → Hg 2+
HC≡C−H H 2 SO 4 → Hg 2+
HC≡C−H H 2 SO 4 → Hg 2+
HC≡C−H H 2 SO 4 → Hg 2+
HC≡C−H H 2 SO 4 → Hg 2+ Acetaldehdye (A)
HC≡C−H H 2 SO 4 → Hg 2+ Acetaldehdye (A) CH
HC≡C−H H 2 SO 4 → Hg 2+ Acetaldehdye (A) CH 3
HC≡C−H H 2 SO 4 → Hg 2+ Acetaldehdye (A) CH 3
HC≡C−H H 2 SO 4 → Hg 2+ Acetaldehdye (A) CH 3 −
HC≡C−H H 2 SO 4 → Hg 2+ Acetaldehdye (A) CH 3 − O
HC≡C−H H 2 SO 4 → Hg 2+ Acetaldehdye (A) CH 3 − O ∣∣
HC≡C−H H 2 SO 4 → Hg 2+ Acetaldehdye (A) CH 3 − O ∣∣
HC≡C−H H 2 SO 4 → Hg 2+ Acetaldehdye (A) CH 3 − O ∣∣
HC≡C−H H 2 SO 4 → Hg 2+ Acetaldehdye (A) CH 3 − O ∣∣ C
HC≡C−H H 2 SO 4 → Hg 2+ Acetaldehdye (A) CH 3 − O ∣∣ C
HC≡C−H H 2 SO 4 → Hg 2+ Acetaldehdye (A) CH 3 − O ∣∣ C −H
HC≡C−H H 2 SO 4 → Hg 2+ Acetaldehdye (A) CH 3 − O ∣∣ C −H
HC≡C−H H 2 SO 4 → Hg 2+ Acetaldehdye (A) CH 3 − O ∣∣ C −H
HC≡C−H H 2 SO 4 → Hg 2+ Acetaldehdye (A) CH 3 − O ∣∣ C −H [O]
HC≡C−H H 2 SO 4 → Hg 2+ Acetaldehdye (A) CH 3 − O ∣∣ C −H [O]oxidation
HC≡C−H H 2 SO 4 → Hg 2+ Acetaldehdye (A) CH 3 − O ∣∣ C −H [O]oxidation
HC≡C−H H 2 SO 4 → Hg 2+ Acetaldehdye (A) CH 3 − O ∣∣ C −H [O]oxidation
HC≡C−H H 2 SO 4 → Hg 2+ Acetaldehdye (A) CH 3 − O ∣∣ C −H [O]oxidation Acetic acid (B)
HC≡C−H H 2 SO 4 → Hg 2+ Acetaldehdye (A) CH 3 − O ∣∣ C −H [O]oxidation Acetic acid (B) CH
HC≡C−H H 2 SO 4 → Hg 2+ Acetaldehdye (A) CH 3 − O ∣∣ C −H [O]oxidation Acetic acid (B) CH 3
HC≡C−H H 2 SO 4 → Hg 2+ Acetaldehdye (A) CH 3 − O ∣∣ C −H [O]oxidation Acetic acid (B) CH 3
HC≡C−H H 2 SO 4 → Hg 2+ Acetaldehdye (A) CH 3 − O ∣∣ C −H [O]oxidation Acetic acid (B) CH 3 −
HC≡C−H H 2 SO 4 → Hg 2+ Acetaldehdye (A) CH 3 − O ∣∣ C −H [O]oxidation Acetic acid (B) CH 3 − O
HC≡C−H H 2 SO 4 → Hg 2+ Acetaldehdye (A) CH 3 − O ∣∣ C −H [O]oxidation Acetic acid (B) CH 3 − O ∣∣
HC≡C−H H 2 SO 4 → Hg 2+ Acetaldehdye (A) CH 3 − O ∣∣ C −H [O]oxidation Acetic acid (B) CH 3 − O ∣∣
HC≡C−H H 2 SO 4 → Hg 2+ Acetaldehdye (A) CH 3 − O ∣∣ C −H [O]oxidation Acetic acid (B) CH 3 − O ∣∣
HC≡C−H H 2 SO 4 → Hg 2+ Acetaldehdye (A) CH 3 − O ∣∣ C −H [O]oxidation Acetic acid (B) CH 3 − O ∣∣ C
HC≡C−H H 2 SO 4 → Hg 2+ Acetaldehdye (A) CH 3 − O ∣∣ C −H [O]oxidation Acetic acid (B) CH 3 − O ∣∣ C
HC≡C−H H 2 SO 4 → Hg 2+ Acetaldehdye (A) CH 3 − O ∣∣ C −H [O]oxidation Acetic acid (B) CH 3 − O ∣∣ C −OH
HC≡C−H H 2 SO 4 → Hg 2+ Acetaldehdye (A) CH 3 − O ∣∣ C −H [O]oxidation Acetic acid (B) CH 3 − O ∣∣ C −OH
HC≡C−H H 2 SO 4 → Hg 2+ Acetaldehdye (A) CH 3 − O ∣∣ C −H [O]oxidation Acetic acid (B) CH 3 − O ∣∣ C −OH .
HC≡C−H H 2 SO 4 → Hg 2+ Acetaldehdye (A) CH 3 − O ∣∣ C −H [O]oxidation Acetic acid (B) CH 3 − O ∣∣ C −OH .Hydration of acetylene (followed by keto enol tautomerism) gives acetaldehdye. This is followed by oxidation to form acetic acid.