D. Hidrazor3. The major organic product which results when PHCHO is treated with the following sequence ofreagents: 1. CH3CH2M9B1; 2. H3O+; 3. Na2Cr207, H2SO4 is:A. PHCOCH3.B. PHOCH2CH3C. PHCH2COCH3D. PHCOCH2CH3Su4. Which of the following is also known as a Schiff base?A. an imineB. a cyanohydrinC. a hydrateD. sodium hydroxideHuluMiniToolPower Dat..COe| support +1-844-865-6999口 || A 2P Type here to searchDELLF10F11F8F9F6F7F3F4F5F1F2Fn

From given Both the question is solved according Initially the sequence is given and schiff base…

3. The major organic product which results when PHCHO is treated with the following sequence of reagents: 1. CH3CH2MgBr; 2. H3O+; 3. Na2Cr207, H2SO4 is: A. PHCOCH3 B. PHOCH2CH3 C. PHCH2COCH3 D. PHCOCH2CH3 4. Which of the following is also known as a Schiff base? A. an imine B. a cyanohydrin C. a hydrate D. sodium hydroxide

3. The major organic product which results when PHCHO is treated with the following sequence of reagents: 1. CH3CH2MgBr; 2. H3O+; 3. Na2Cr207, H2SO4 is: A. PHCOCH3 B. PHOCH2CH3 C. PHCH2COCH3 D. PHCOCH2CH3 4. Which of the following is also known as a Schiff base? A. an imine B. a cyanohydrin C. a hydrate D. sodium hydroxide

Organic Chemistry

8th Edition

ISBN:9781305580350

Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Chapter10: Alcohols

Section: Chapter Questions

Problem 10.57P

See similar textbooks

Similar questions

A chiral amine A having the R conguration undergoes Hofmann elimination to form an alkene B as the major product. B is oxidatively cleaved with ozone, followed by CH3SCH3, to form CH2 = O and CH3CH2CH2CHO. What are the structures of A and B?
( give clear handwritten answer )give effiecient synthesis route for following with detailed meechanism.
Explain the E2 mechanism (bimolecular elimination) of of Elimination ?
To prepare butanoic acid from 1-propanol, which sequence of reagent(s) is/are best employed? a) (1) NaCN; (2) H2O; (3) [H+] b) LiAlH4 c) K2Cr2O7 in acid d) (1) PBr3; (2) NaCN; (3) H2O; (4) [H+]
Which reagent(s) sequence(s) is/are optimum for preparing butanoic acid from 1-propanol? i. K2Cr2O7 in acidii. (1) PBr3; (2) NaCN; (3) H2O; (4) [H+] iii. (1) NaCN; (2) H2O; (3) [H+]iv. LiAlH4
Explain the reaction for the formation of acetal and hemiacetal. Explain why N,N-disubstituted amide is less acidic than ester. Why only methyl ketone do undergoes haloform reaction. LDA is the base of choice for carbonyl compound to completely convert into enolate. Why?
Quinapril (trade name Accupril) is used to treat high blood pressure andcongestive heart failure. One step in the synthesis of quinapril involvesreaction of the racemic alkyl bromide A with a single enantiomer of theamino ester B. Given the structure of quinapril, which one of these two products isneeded to synthesize the drug?
1. The of alka zeltzer in iced water will give a result and observation of _________. alka zetltzer dissolved readily alka zeltzer partially dissolved No reaction 2. In the Le Chatelier's Principle, Co(H2O)6 with oxidation of +2 is _________ in color. blue violet pink
Interestingly, reduction of the complex shown above mostly gives thealcohol enantiomer shown below after workup. a. Draw the other minor diastereomeric alcohol product. b. Briefly explain the diastereoselectivity of the reduction – why is oneenantiomer heavily favored? Draw a structure or structures to support youranswer.
The analgesic acetaminophen is synthesized by treating 4-aminophenol with one equivalent of acetic anhydride. Complete the equation for the formation of acetaminophen. a. Acetaminophen: b. Additional Product pls add the name for both, thanks!
Organotin compounds play a significant role in diverse industrial applications. They have been used as plastic stabilizers and as pesticides or fungicides. One method used to prepare simple tetraalkylstannanes is the controlled direct reaction of liquid tin(IV) chloride with highly reactive trialkylaluminum compounds, such as liquid triethylaluminum (Al(CzHs)3). 3SnCl4 + 4Al(C2H5)3 → 3Sn(C2H5)4 + 4AlCl3 In one experiment, 0.160 L of SnCl4 (d= 2.226 g/mL) was treated with 0.346 L of triethylaluminum (Al(C2H5)3); d = 0.835 g/mL). What is the theoretical yield in this experiment (mass of tetraethylstannane, Sn(C2H5)4)? If 0.257L of tetraethylstannane (d= 1.187 g/mL) were actually isolated in this experiment, what was the percent yield?
Using any necessary organic and inorganic reagents, show how you can carry out the chemical conversions shwon below. Please answer parts a, b, and c.