Please show the FULL mechanism with curved arrows showing the oxidation of benzydrol to benzophenone, using NaCIO. The phase transfer catalyst should NOT be included (Bu4NHSO). I am having a hard time visualizing this. The mechanism should look similar to the oxidation of cyclohexanol. The balanced equation is provided: OH NaCIO, BU NHSO4 EtOAC (ethyl acetate) Benzhydrol Benzophenone Thank you!!

Please show the FULL mechanism with curved arrows showing the oxidation of benzydrol to benzophenone, using NaCIO. The phase transfer catalyst should NOT be included (Bu4NHSO). I am having a hard time visualizing this. The mechanism should look similar to the oxidation of cyclohexanol. The balanced equation is provided: OH NaCIO, BU NHSO4 EtOAC (ethyl acetate) Benzhydrol Benzophenone Thank you!!

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

See similar textbooks

Similar questions

Question 17 Consider the mechanism that converts the starting material to the product and identify the true statement. OCH, OCH3 a CH CH,CI AICI3 The electrophile generated is the methyl carbocation. The substitution is ortho because the methyl group stabilizes the positive charge that develops in the on carbon b by induction. The substitution is ortho because the methoxy group stabilizes the positive charge that develops on carbon a by resonance. A proton is removed from carbon c to re-aromatize the ring.
write chemical equations for the preparation of the following compounds either diethy monolatmonolayer or ethyl acetoacetate Write chemical equations for the preparation of the following compounds from either diethyl malonate or ethyl acetoacetate: a' t c) -149 1. Write chemical equations for the preparation of the following compounds from either diethyl malonate or ethyl acetoacetate: CH2CH2CCH3 a) -CH2CH2CO₂H c) HO₂CCH2CHCO₂H d) CH3 H3C CH2CO₂H
Identify the product obtained in the hydrolysis of the following cyclic acid anhydride. CH₂ A) HOT B) C) НО D) HO H₂O, HCI (complete hydrolysis) w O OH + CH₂NH₂& H OH OH CH, SH,& CHÍNH CHÍNH CH
Synthesis of Dilantin by Multi-Step Synthesis Part 4 - Ureabenzil Condensation Table of Reagents Molecular weight (g/mol) Mass (g) Volume (mL) density (g/mL) Amount (mmol) Reagent benzil 210.23 1.0 4.75 Sodium hydroxide (30% wv) 39.997 1.2 loo urea 0.432 7,19 - Limiting Reagent: Identify the limiting reagent (warning, some reagents may be catalysts, and can be used in sub- stoichiometric amounts, and not all reactions have 1:1 stoichiometric coefficients) Yield of Product: Calculate the % yield of product you obtained. Watch significant figures and SHOW YOUR WORKING. Overall yield of product based on benzaldehyde: Calculate the % yield of the product you obtained based on the starting material for this synthesis, benzaldehyde. Watch significant figures and SHOW YOUR WORKING.
So I’m supposed to write a chemical equation, then draw the structures, of the preparation of phenacetin starting from 4-ethoxyaniline. Would the correct equation be 4-ethoxyanilime + acetic anhydride (right arrow) phenacetin + CH3COOH? Or am I totally wrong? Thank you!
S S tos es S es para estos sy no s? rometano utanol butanal X O 14 Which of the following compounds is one of the best solvents for polar and nonpolar compounds? dichloromethane 1-butanol 1-butanal acetone ww hp Fe Pro Tan WhatsA
uestion 40 What is the major organic product obtained from the following reaction? NaOH, H20 1 а. 1 O b. 2 с. 3 4 d. 4 Moving to another question will save this response. e Type here to search ОООО
1c. What is the nucleophile in the following reaction? .Br CH;CO0 Na LO OCCH3 NaBr ld. What is the electrophile in the following reaction? Br CH;COO Na L0OCCH3 NaBr +
Provide the correct systematic name for the compound shown here. H3C (Z)- Question 2 of 14 3- NH₂ CH3 CH3 (S)-(E)- (R)- 4- 6- 5- 2- cyclo tri di sec- tert- iso nitro meth but amino prop hex Submit +
B. Supply the missing product or reagent for the following reactions OH ОН OH PCC POCI3,, pyridine HBr, heat OH OH Br Mg H₂SO4, heat 1) NaH 2) Ph Br
sch 9 Stu H We S 回Brca Am G CH Q O lov CH Ca M cer C Ch ML Ser O File | C/Users/watsa/Downloads/HW_Problems_Ch 15 7th edition%20(2).pdf V Draw E | D Page view A Read aloud D Add text 3 Draw the structural formula of the organic product or indicate that no reaction occurs for the following situations. a. Propanal in the Tollens test b. 3-Pentanone in the Tollens test c. Methylpropanal in the Benedict's test d. Propanone in the Benedict's test 5-79 What is the chemical formula of the inorganic product formed, if any, in each of the reactions in Problem 15-77? 15-80 What is the chemical formula of the inorganic preduct formed, if any, in each of the reactions in Problem 15-78? Type here to search DELL F4 F5
ANAL 728: Identifying an Unknown Aldehyde or Ketone 4. In the procedure for preparing semicarbazone derivatives, what is the pur- pose of adding sodium acetate to semicarbazide hydrochloride? TAE MOIT EMAN SHoS 10 shysshlA ruoolrU nn gniytiinshl18STJAMA InsmngizaA yiolsTodsl-911