Answered: Identify the MAJOR product that would…

Identify the MAJOR product that would be obtained from the following reaction. Hint - sodium thiophenolate (Na+ -SPh ) is a good nucleophile. NaSPh (S)-2-iodopentane

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

Chapter9: Nucleophilic Substitution And Β-elimination

Section9.9: Analysis Of Several Competitions Between Substitutions And Eliminations

Problem CQ

See similar textbooks

Related questions

Q: Devise a synthesis of 1-pentyne using one of the starting materials and any of the reagents below…

A: Synthesise the 1pentyne from suitable alkyne and select suitable reagents

Q: (CH3)3CBR + H2O → (CH3)3COH + HBr What is the effect of doubling both the t-butyl bromide and water…

A: SN1 reaction is the nucleophilic substitution unimolecular. First step is the formation of…

Q: 2. Cyclic esters are usually called lactones. They also undergo double Grignard additions leading to…

A: When an ester reacts with an excess of a Grignard reagent, the final product is a tertiary alcohol.…

Q: Which of the following compounds could have been the original carbonyl compound in the synthesis of…

A: Applying concept of organic synthesis of given compound.

Q: Give the major product(s) of the following reaction. PBR3, heat CH3CH2OH pyridine

A: The reaction is given as,

Q: Choose the best reagents from the list provided below for carrying out the following conversion.…

Q: What would be the product if (S)-2-bromobutane underwent an S№1 reaction wit water in the presence…

A: As this is proceeds through SN1 reaction, so it form planar carbocation, now nucleophile will attack…

Q: Be sure to answer all parts. What is the major product formed when the following alkyl halide is…

A: The question is based on organic reactions. We need to identify the product and explain its…

Q: Propose an efficient synthesis for the following transformation: ? SH The transformation above can…

A: Transformation of cyclopentane to cyclopentanethiol : 1. Halogenation of Cyclopentane:Reagent: G…

Q: Which of the following statements is true about the reaction below? CH3CH2OH The carbocation is an…

A: Given chemical reaction is:

Q: Give the major product of the following reaction. OH Na2Cr,07 H,SO4

Q: ropose an efficient synthesis for the following transformation: -> ACDCEF The transformation above…

A: The question is based on the concept of organic synthesis.We need to synthesize the product using…

Q: -which would be the best way to carry out the following synthesis? CH-CH-CH, CH-CH-CH,OH Br

Q: From the table of available reagents select the one(s) you would use to convert cyclohexanone to the…

Q: CH3 CH3 Strong Bulky base Heat Br

A: Answer

Q: Propose an efficient synthesis for the following transformation: HO (b) The transformation above can…

A: We have to carry out the given transformation. And given the sequence of the required reagents.

Q: BuLi -Br Ph3P A В + ↑

A: This reaction is Wittig reaction. Alkene is produced from carbonyl group.

Q: 1. NaOMe Br(CH₂) 3Br 2. LDA (H₂O) 1. Me,NH cat. H+ 2. Me A CO₂Et

A: LDA and NaOMe are bases which abstract acid protons.LDA is bulky base which selectively abstract…

Q: 2. Predict the product(s) that forms and explain why it forms. Assume that any necessary catalytic…

A: Since you have posted a question with multiple questions, we will provide the solution only to the…

Q: Propose an efficient synthesis for the following transformation: CN -) The transformation above can…

Q: 3 Treatment of 1-aminoadamantane, C„H„N, with methyl 2,4-dibromobutanoate in the presence of a…

A: In the given SN2 reaction, 1-aminoadamantane act as a nucleophile and it make a bond with terminal…

Q: Propose an efficient synthesis for the following transformation: Br Br The transformation above can…

A: answer is BICA It is a multi step organic synthesis Involves nucleophilic substitution Birch…

Q: Which reagents would best carry out the following transformation? H₂, Lindlar's catalyst Na, NH3 O…

A: Alkyne react with lindlar Catalyst and gives syn alkene

Q: Which statement best characterizes the following reaction of 2-phenylpropan-2-ol with HBr? OH CH3…

A: An arrow always depicts from a region of high electron density to low electron density ; that is…

Q: Using a retrosynthetic approach, develop a synthesis of the given hydrocarbon. Part: 0/3 Br Part 1…

A: The retroanalysis for the target molecule is as follows:

Q: OCH3 ? 0 0 OCH 3 A NaH B NaOH C NaOCH 3 D NaOCH₂CH3

Q: Provide the bond line structures for all the enols the y-diketone CH3COCH2C(CH3)2COCH₂CH3 can form.…

A: enols can be drawn by converting ketone group to OH followed by adjacent double bond (alkene) group.

Question

Identify the MAJOR product that would be obtained from the following reaction.
Hint - sodium thiophenolate (Na+ -SPh ) is a good nucleophile.
NaSPh
(S)-2-iodopentane

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

Knowledge Booster

Learn more about

Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.

Similar questions

Identify the MAJOR product that would be obtained from the following reaction. Hint - sodium thiophenolate (Na+ -SPh) is a good nucleophile. Na SPh (S)-2-iodopentane SPh SPh + enantiomer ŠPh SPh SPh
Give me a clear handwritten answer
What is the nucleophile in the following reaction? 2H2 0 + CH3! → CH3OH +F + H3O* 12 O CH3I O CH3OH O H3O*
All but one of these functional groups must be excluded from Grignard reagents or the carbonyl compound they react with because it will neutralize them. O alcohol (ROH) O terminal acetylene (R-C=CH) O carboxylic acid (R-CO₂H) Oether (R-O-R)
In hydrobromination of 3-hexene, which of the following pairs of species act as nucleophiles? 3-hexene, Br– 3-hexene, HBr HBr, Br– HBr, Br2
The reaction of 1-bromobutane with which of the following nucleophiles is a carbon chain-lengthening reaction? sodium acetylide (NaC=CH) sodium hydroxide (NaOH) O ammonia (NH3) potassium iodide (KI)
Rationalize the selectivity observed in the benzil reduction. Draw the transition states of the nucleophilic attack leading to either meso or racemic products and indicate why one is more stable than the other.
Which of the following is more nucleophilic and why? CH30 (CH3)3CO 1 2 Compound 2, because its nucleophilicity is increased by the adjacent CH3 groups. Compound 2 because it is a stronger base. Compound 1, because the nucleophilicity of compound 2 is decreased by steric effects. Compound 1, because it has a weaker conjugate acid. O They actually have about the same nucleophilicity since in both, the negative charge is localized on an oxygen atom.
For the reaction shown below, add arrows to indicate the movement of electrons. In the reaction, does the enolate act as the electrophile or as the nucleophile?
How does the negative inductive effect (−I) of chlorine in the ortho position of the phenol, reduce the negative charge, located on the oxygen of the phenolate anion? Is this why the Oxygen in the phenolate ion will act as a worse nucleophile if the Chlorine is in the ortho position vs the para position?
Choose the nucleophile best suited for the conversion of an acid chloride to a carboxylic acid. na NaOCH3 CH3NH2 H₂O CH3OH ? OH
When a single compound contains both a nucleophile and a leaving group, an intramolecular reaction may occur. With this in mind, draw the product of the following reaction