Incorrect, 2 attempts remaining H+ OH CH3CH2OH2+ :0 protonation Draw Intermediate CH3CH2OH nucleophilic addition Ö H CH3CH2OH deprotonation Draw the Hemi-acetal Draw Intermediate CH3CH2OH2 protonation CH3CH2OH2 1 protonation H -H₂O :0: elimination Draw Intermediate Draw Intermediate H CH3CH2OH CH3CH2OH nucleophilic addition deprotonation Draw Product Draw Intermediate esc F1 80 F2 000 000 F3 F4 F5

Q: 요.. CHJOH H* H* 마음 hemiacetal hemiacetal hemiacetal (excess) TSOH CH, OH HP CH₂OH (excess) H2SO4…

A: Given,

Q: Draw Reaction mechanism for ephedrine. Left one is the example for aspirin

A: Reaction mechanism for ephedrine:- There are many methods or ways of preparation for ephedrine.

Q: Draw the mechanism of the transformation from 3 to 4. F EtO HO 3 OEt NaOH, MeOH HO OH

A: The objective of the question is to understand the mechanism of the transformation from compound 3…

Q: Which of the following is a keto-enol tautomeric pair? HDJCMD O A) B) C) OH

A: Answer:- This question is answered by using the simple concept of Keto enol isomerism in which keto…

Q: O The O atom in the carbonyl (C=O) group the C atom in the carbonly (C=O) group Any H atom Catom not…

A:

Q: Click on the highlighted areas in these molecules to indicate the presence of electropihilic…

A: Nucleophile is a species which is electron rich. It has having negative charge or lone pair of…

Q: Draw the structure of 3-ethoxy-5-hydroxyhept-6-en-2-one. Select Draw Rings More C H

A: In this question we have to tell the structure of 3-ethoxy-5hydroxyhept-6-en-2-one.

Q: 1. Draw a stepwise mechanism for the following addition reaction to an alkene. a) b) c) H 8 + + 0₂…

A: The free radicle reactions are those who doesn't required any catalyst. They can be initiated by…

Q: OH H3O* H20 он or он „CH3 H20 CH3 он

A: The mechanism for the following reaction is-

Q: Macmillan Learning Classify each molecule as an aldehyde, ketone, or neither. Incorrect Aldehyde CH…

A:

Q: Curved arrows are used to illustrate the flow of electrons. Follow the arrows and draw the missing…

A: Here we are required to find the intermediate and the product of the reaction.

Q: Draw

A: This reaction is called Wittig Reaction because Ketone Carbonyl compound react with phosphoylide.

Q: Q2-) Draw a detailed mechanism for the following Fischer esterification reaction.(13 points) A few…

A: When acetic acid and ethanol react in the presence of concentrated H2SO4 they give rise to a sweet…

Q: Please correct answer and don't use hend raiting

A: The reaction is acid-catalyzed hydration. It is an alkene addition that proceeds in Markovnikov…

Q: Which is an appropriate name for the following compound?

A:

Q: Choose the correct product of the following reaction. A Ph- -CH2CH3 H H Select one: Ph CH2CH3 Ph…

A: Given,

Q: Propose syntheses of acetals A and B from carbonyl compounds and alcohols. Draw the structures of…

A:

Q: Show how hydrogen bonding occurs between acetone and water. CH3 C CH3 H₂O

A:

Q: iew Available Hint(s) Hemiacetals Н 0 HO Acetals CH₂OH OH HO OH 0 CH2OH ОН OH OH о + 0 Neither

A: Acetal-: It is a functional group in which a carbon atom bonded to two alkoxy group(-OR) is called…

Q: Draw the Reactant H₂C H 0: O-CH3 CH3OH2 protonati on CH3OH₂ protonation CH3OH deprotonation H₂C H…

A: This an example of ketal protection

Q: Draw the mechanism of the transformation from 3 to 4. F EtO HO 3 OEt NaOH, MeOH HO OH

A: The objective of the question is to understand the mechanism of the transformation from compound 3…

Q: OH H30* H20 OH OH CH3 H20 CH3 OH

A:

Q: OMe OMe tert-Butanol H2SO4 Acetic acid OMe OMe

A: Below attached file showing the details step wise mechanism to the given reaction.  All the best.

Q: Choose the best reagents to complete the reaction shown below. Br

A:

Q: CH₂ CH₂

A:

Q: NaOH H;C--o-CH3 H;C- Na но-сн, + H20

A: Addition of nucleophile  Loss of leaving group  Proton transfer

Q: Draw the end product(s) of each reaction.

A: Reaction of 1,1-diol react with an acid to give corresponding carbonyl compounds. Ketals undergo…

Q: Br CH3 CH3 CH3OH heat CH3 CH3

A: E1 elimination reaction follows through formation of carbocation intermediate.

Q: product and explanation

A: Step 1:The given reaction produces a substitution product with the phenoxide ion (PhO-) attacks the…

Q: Reaction 1: مرة -c 1) NaOH a) Bra in CH₂Cla OH

A: Alpha halo ketone react with NaOH to form carboxylic acid compound. In this reaction, ring…

Q: QUESTION 30 What is the product of this aldol condensation? H₂C H₂C a) H₂C- b) + H₂C- CH,…

A:

Q: e) decarboxylation O || CH3CH₂-C-0-H f) 1! CO₂ ? CH3 CH3 + CO₂

A: Any Carboxylic acid on strong heating undergo decarboxylation to give alkane and CO2 gas

Q: The intermediate formed in the previous step is resonance-stabilized. Draw the missing curved…

A: