Although alcohol V gives a single alkene W when treated with POCI, and pyridine, three isomeric alkenes (X-Z) are formed on dehydration with H,SO4. Draw a stepwise mechanism for each reaction and explain why the difference occurs. он do.do.de POCI, pyridine V w H2SO4

Although alcohol V gives a single alkene W when treated with POCI, and pyridine, three isomeric alkenes (X-Z) are formed on dehydration with H,SO4. Draw a stepwise mechanism for each reaction and explain why the difference occurs. он do.do.de POCI, pyridine V w H2SO4

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

Related questions

Q: What alkenes are formed when attached alcohol is dehydrated with TsOH?Label the major product when a…

A: Given,

Q: Draw the products in each reaction. CH,CH3 CH;CH,OH K* -OC(CH,)3 а. Он CH3CH2O b. CH3-C-CH,CH3 d. CI

A: Since you have posted a question with multiple sub-parts, we will solve first three sub-parts for…

Q: Draw a stepwise mechanism for the following reaction.

Q: Draw a stepwise mechanism for the following reaction. CH3 H C-CH3 CH3-C- CH, H HBr CH3-C -C-CH3 + Hо…

A: The given reaction is,

Q: What alcohol is formed when each compound is treated with NaBH4 in CH3OH?

Q: Draw a stepwise mechanism for each reaction.

Q: N° `Ph cat. H* А +В Ph -H,0 HO. CI

Q: Synthesize each compound from toluene and any other organic or inorganic reagents. a. CsHsCH2Br b.…

A: Synthesis of the targeted compound can be done in different ways. But, here I am showing the most…

Q: Draw the products formed when each compound is treated with HNO3 and H2SO4.

A: EXPLANATION: a) part -OCH3 is ortho, para director whereas -COOCH3 is a meta director.Because -OCH3…

Q: Draw the organic product(s) formed when CH3CH₂CH₂OH is treated with each reagent. a. H₂SO4 d. HBr b.…

Q: Synthesize each compound from benzene.

Q: Dimethyl cyclopropanes can be prepared by the reaction of an α, β- unsaturated carbonyl compound X…

Q: Draw a stepwise mechanism for the following reaction.

Q: Give the IUPAC name of each alcohol.

Q: Draw the product formed when each compound is treated with two equivalents of CH;CH,CH,CHgMgBr…

A: CH3CH2CH2CH2MgBr also known as n-butylmagnesiumbromide is a Grignard reagent that is a rich source…

Q: What alcohol is formed when each compound is treated with H 2 and a Pd catalyst?

A: When alcohol or ketone reacts with H2 and Pd catalyst then alcohol reduce to primary alcohol and…

Q: What ester is formed when each carboxylic acid is treated with ethanol (CH 3CH 2OH) in the presence…

A: Esters are formed by the reaction of carboxylic acid with alcohol in the presence of catalytic…

Q: Be sure to answer all parts. Draw the organic product formed when pentanoyl chloride…

A: We have to identify the product. The given reagents are as follows - Pentanoyl chloride CH3CH2…

Q: Devise a synthesis of each compound from CH3CH2CH2CO2Et, benzene, and alcohols having ≤ 2 C's. You…

A: EXPLANATION: part a) First compound synthesis: In First step, there is conversion of benzene to…

Q: Draw a stepwise mechanism for the following reaction. C(CHa)3 AICI, (CH3)2CHCH,CI HCI

Q: What product is fomed when each alkene is treated with HCI? CH3 à. b. CH3CH,CH2CH=CHCH,CH,CH3 C. CH3

Q: Draw a stepwise mechanism for the following reaction. (Hint: Two Michael reactions are needed.)

A: Given reaction:

Q: Starting with bromocyclohexane, how can each of the following compounds be prepared?

A: Since we only answer up to 3 sub-parts, we’ll answer the first 3. Please resubmit the question and…

Q: 5. What reagents are needed to convert toluene (C,H,CH,) to each compound? a. C.H₂COOH c.…

A: Since you have posted a question with multiple sub-parts, we will solve the first three subparts for…

Q: Draw a stepwise mechanism for the following isomerization.

A: A stepwise mechanism for the given isomerization can be drawn as

Q: PLEASE HELP Draw the products formed when cyclohexene is treated with each reagent

Q: I. What products are formed when each alcohol is oxidized with K2Cr207? a. CH;CH,CH2CH,CH2OH ОН ОН…

A: Concept: 1) K2Cr2O7 is a powerful uncontrolled oxidizing agent. 2) primary alcohol is converted…

Q: 8. Name the following ethers. b) a) CHS-0-CH3 CH-0-CH-Cty d) CHy-0-CHCHy CH_ CH c) CAy-CH-

A: Ethers are the organic compounds, where Carbon-Oxygen- Carbon bond is found. These compounds are…

Q: What product is formed when each compound undergoes an intramolecular reaction in the presence of…

A: Intramolecular reactions are those reaction which takes place within a molecule. Many types of…

Q: What ester and Grignard reagent are needed to synthesize each alcohol?

A: The first compound can be prepared for the ester named methyl-4-methyl pentanoate and2 moles of…

Q: d. CH3CH₂CH₂CH₂OH e. он

A: P-tolylsulphonic acid after giving H+ is quite stable due to its resonating structure and hence the…

Q: Provide all possible products formed in the given reaction Draw the products formed when each ether…

A: When ether react with one equivalent HBr then alcohol and alkyl bromide is formed but when 2…

Q: An allylic alcohol contains an OH group on a carbon atom adjacent to a C—C double bond. Treatment of…

A: The given reaction occurs via the formation of carbonation and this carbonation undergoes…

Q: Draw a stepwise mechanism for the following reaction that forms ether D. D can be converted to the…

Q: Draw a stepwise mechanism for the attached reaction that forms ether D. D can be converted to the…

A: It is given that alcohol and an alkyl halide substrate are reacting to form an ether D, and further,…

Question

Although alcohol V gives a single alkene W when treated with POCI, and pyridine, three isomeric alkenes (X-Z) are formed on
dehydration with H,SO4. Draw a stepwise mechanism for each reaction and explain why the difference occurs.
он
do.do.de
POCI,
pyridine
V
w
H2SO4

Expert Solution

This question has been solved!

Explore an expertly crafted, step-by-step solution for a thorough understanding of key concepts.

This is a popular solution!

SEE SOLUTION Check out a sample Q&A here

Step 1

VIEW

Step 2

VIEW

Trending now

This is a popular solution!

Step by step

Solved in 2 steps with 2 images

SEE SOLUTION Check out a sample Q&A here

Similar questions

Chemistry
Dimethyl cyclopropanes can be prepared by the reaction of an α, β-unsaturated carbonyl compound X with two equivalents of a Wittigreagent Y. Draw a stepwise mechanism for this reaction.
Draw a stepwise mechanism for the following reaction, a key step in the synthesis of the anti-inflammatory drug celecoxib (trade name Celebrex).
What alkenes are formed when each alcohol is dehydrated with TSOH? Label the major product when a mixture results. OH Xom OH a. OH b. CH₂CH3 OH C. d. CH₂CH₂CH₂CH₂OH e.
Draw the products formed when each alkene is treated with O3 followed by Zn, H2O.
Synthesize each compound from cyclohexanol, ethanol, and any other needed reagents.
Help me please sir/ma'am
What products can be formed when each alcohol is:
Draw the structure of the product from the following: 1-Octyne + BH3 --> A A + H₂O₂/NaOH --> B Draw the structures of A and B
Draw the products of each elimination reaction.
Give the IUPAC name for each nitrile.
Draw the product formed when pentanal (CH3 CH₂ CH₂ CH₂ CHO) is treated with each reagent. With some reagents, no reaction occurs. a. NaBH4, CH3OH b. [1] LiAiH4: [2] H₂O c. H₂, Pd-C d. PCC e. Na₂Cr₂O7, H₂SO4, H₂O f. Ag₂O, NH4OH g. [1] CH3 MgBr; [2] H₂O h. [1] C6H5 Li: [2] H₂O i. [1] (CH3)2 CuLi; [2] H₂O J. [1] HC=CNa; [2] H₂O k. [1] CH 3 C=CLI; [2] H₂O 1. The product in (a), then TBDMS-CI, imidazole