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. Na SPh (S)-2-iodopentane SPh SPh + enantiomer ŠPh SPh SPh

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 is the best choice of reagent to perform the following transformation? Xar -x O NaOH OHCI O…

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

Q: Either enantiomer of the SULFOXIDE below may be prepared from (S)-2-butanol. Propose an efficient…

A: So according to question , we will provide the suitable reagents and synthetic process of each…

Q: Rank the following carbonyl compounds in order of increasing reactivity towards nucleophiles: NH2 I…

A: For the Carboxylic acid derivative like amide, ester and acid anhydride the nucleophilic…

Q: Which reagent would you use to accomplish each of the following transformations? Options (please…

A: Reagent 1: H2O-H2SO4 Reagent 2: O3-Me2S Explanation:Step 1: Reaction Step 2: MechanismReaction 1 is…

Q: Benzene was treated with hot a mixture of the bromo compound (A) and aluminum bromide (AIBr3). Upon…

Q: .CH3 CH2CI2 H3C Br2 (1 mole) +

A: In the above reaction there is addition of electrophilic addition of bromine in presence of…

Q: Predict the reagent(s) needed to produce this product. A с D H₂ Pt |- H₂ H₂O Pd/C H₂O HCI

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

Q: which of the following solvents will best promote a nucleophilic reaction between NaCN and…

A: Polar aprotic solvents such as DMSO, acetone, DMF and acetonitrile are often chosen for SN2…

Q: Match the reagent on the left in the list below with the product formed on the right when the…

A: Reaction 1: cyclohexanone reaction with Hydroxyl amine gives oxime. Reaction 2: Cyclohexanone…

Q: Identify the MAJOR product that would be obtained from the following reaction. Hint - sodium…

Q: Br2 (g) FeBr3 CI CI Br2 H2NNH2 В C (h) A FeBr3 AICI3 OH (Give all products) NH2 HNO3 (i) H2SO4

A: #(g): Br2/FeBr3 add a -Br group to a benzene ring. The reactant has two groups attached which are:…

Q: Identify reagents that can be used to achieve the transformation shown. 9 OH ? OH OLIAIH4 O PCC,…

Q: 1-Hexyne is treated with sodium hydride, followed by bromoethane. Lindlar hydrogenation of the…

A: Given :

Q: Rank these substrates in order of increasing ability to undergo a nucleophilic substitution aromatic…

Q: Propose an efficient synthesis for the following transformation: OH Ph H 1) MeMgBr 2) H3O+ D Ph The…

Q: Propose a structure(s) for the product(s) of the following reactions. H2SO4, HNO3

Q: H3C- OH H ACO H 00 XIII Dess-Martin periodinane provides a means to oxidize a primary alcohol to an…

A: Organic compounds can be defined as compounds that contain carbon and hydrogen atoms. The carbon…

Q: Which of the following bases gives the highest Zaitsev product in an E2 reaction with…

Q: Bromohydrin 1 can be prepared from the alkene shown below by reaction with Br2 and H20 as shown…

Q: Which of the following reagents would NOT convert the starting material to the shown product? ??? OH…

A: c

Q: 1. An alkyl chloride is treated with lithium diisopropyl amide, forming the following two products.…

Q: Which reagent would you use to accomplish each of the following transformations? Options (please…

A: Reagent 1: O3-Me2S Reagent 2: MCPBA-H3O+ Explanation:Step 1: Reaction Step 2: MechansimReaction 1 is…

Q: CH3 CH3 Strong Bulky base Heat Br

A: Answer

Q: Identify the MAJOR product that would be obtained from the following reaction. Hint - sodium cyanide…

Q: Draw the major organic product of the reaction shown below. -OH K₂Cr₂07 H₂SO4, H₂O • You do not have…

Q: Which of these structures fit the following descriptions? An alkyl halide that gives a mixture of…

A: The given alkyl halide can only give mixture of two alkene.Therefore, it is wrong description (1).

Q: 1. Provide the major product(s) for the following reactions. Be sure to indicate stereochemistry…

Q: A 16. The major monobromination product in the following reaction is

A: Given : reactant Tip : stability of carbon free radical is 3°>2°>1°

Q: Ticlopidine is an antiplatelet drug used to prevent strokes. Draw an alkyl halide and choose the…

A: Alkyl halide reacts with ammonia to form a primary amine. Alkyl halide reacts with a primary amine…

Q: Which reagents afford the transformation shown? C H2, Pt H2, Lindlar's catalyst C Na, NH3 C H2, Pd C…

Q: All but one of these functional groups must be excluded from Grignard reagents or the carbonyl…

A: The question is based on the concept of organic reactions. we need to identify the functional group…

Q: Br HO, O H20, SOCI2 O H20, H2SO4 O NAOH, H20 then H3O* O NaOMe, MEOH

A: The best reagent to accomplish the given reaction is as follows :

Q: Determine reagents C and D from the reaction scheme below. Choose two (2) answers. Select one or…

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

Q: Which of the following is more nucleophilic and why? CH30 (CH3)3CO 1 2 Compound 2, because its…

A: Strong nucleophile means an atom or a group carry lone pair of electrons. It effectively go to…

Q: I am having trouble figuring out what regent can be used to get the product. This is what I have so…

A: Organic reactions are those in which organic reactant react to form organic products. In the given…

Q: 1. Predict the product of each reaction below

A: Given are organic reactions. Given starting compound is alcohol.Note: According to our guidelines we…

Q: Treatment of the following stereoisomer of 1-bromo-1,2- diphenylpropane with sodium ethoxide in…

A: E2 elimination is a second order reaction.It is a concerted reaction where simultaneous abstraction…

Question

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

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

Which of the following compounds would be capable of undergoing a nucleophilic aromatic substitution reaction upon reaction with a good nucleophile? Br & I Compound IV only Compounds I, III and IV O Compounds I and III O Compound II only CI Br II Br III Br IV
Please provide a curved-arrow mechanism for the following reaction. Be sure to use your mechanism and a few words to explain the regiochemistry of the bromines in the final product and why each carbocation intermediate in your mechanism is the preferred intermediate for that step. Include ALL lone pairs and formal charges. Thank you.
Show the reagents for the conversion below: он OCH3 NO2
Which of the following reagents is best to achieve the given transformation? H₂C 0=s=0 0000 → KOtBu OCH3OH NaOH TsCI, Py
What is the most likely name of this thiol ester; CH3-CH(-CI)-C(=O)-S-CH₂-CH(-Br)-CH₂-CH(-CH3)-CH2-CH3 4-bromo-2-methyl-2 chloropropyl thiohexanoate None of these 2-bromo-cyclohexyl 3-chloro-2-thiolpropanoate 2-bromo-4-methylhexyl 2-chloro-thiopropanoate 2-chloropropyl 3-bromo-3-methylhexanoate
Draw the structural formula for the major product(s) resulting from the following reactions
Write a series of steps to convert 1-hexanol to 3-chlorohexan-2-one via an enolate intermediate. H3C مینه وال لها H ОН H3C CH .CH3
Indicate the products or reagents of the following transformations.
What are the best reagents to accomplish this transformation? ? Br NaCE CH, followed by H2 and Pt NaCE CH, followed by H2 and Lindlar's catalyst NaOH, followed by t-BuOK t-BuOK
Draw the major organic products obtained from the reactions below. Be mindful of stereochemistry and regioselectivity. If stereochemistry is included in the product, note that the diast/enant is also included, but not provided due to space. Assume one equivalent unless stated otherwise, or if the reagent is a solvent, oxidant or reductant.
Please show reaekson and don't use hend raiting