Give the organic product:H-S-CH,CH3(HINT: "S" is a nucleophile )S-CH,CH3-S-CH2CH3AОНS-CH2CH3BDНОCH3CH2-SSelect one:ВA

Here S is a nucleophile,attack at carbon and remove at the oxygen site,so oxygen become -ve charge…

Answered: H-S-CH,CH3 (HINT: "S" is a nucleophile…

Science

Chemistry

H-S-CH,CH3 (HINT: "S" is a nucleophile ) S-CH2CH3 -S-CH2CH3 C А ОН S-CH2CH3 B D HO CH3CH2-S Select one: A

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

Chapter16: Aldehydes And Ketones

Section: Chapter Questions

Problem 16.45P: The following bicyclic ketone has two -carbons and three -hydrogens. When this molecule is treated...

See similar textbooks

Related questions

Q: Which of the following reagent best accomplish this transformation below? CH CH- CEC- A (1st) HCI,…

Q: 7. Which nucleophile would you expect to add reversibly to an a,ß-unsaturated carbonyl? а. NaBHa b.…

A: Addition of a nucleophile to an α,β-unsaturated carbonyl compound Takes place in two ways; one is…

Q: Which molecule can loose a hydrogen and become a nucleophile? Select one: a. H3C– ECH b. H;C- -CH3…

A: The terminal alkynes or 1-alkynes are weak acids and loose a hydrogen when treated with strong base…

Q: Which compound in each pair reacts faster in nucleophilic substitution? a. CH;CH2CH2CI or CH;CH2CH2I…

A: Given pairs, a. CH3CH2CH2Cl or CH3CH2CH2I b. (CH3)3CBr or (CH3)3CI c. (CH3)3COH or (CH3)3COH2+…

Q: A set of three nucleophilic displacement reactions is shown below: Br Br CH3 CH3CHCH2CH2CH2CH3…

Q: z. hex-4-en-3-one + CH3CH2MGBR 1. React the carbonyl compound: It is (circle one)CONJUGATED…

A: As there are two questions, we are solving all three parts of the first question for you, for the…

Q: Reagents required to carry out the following transformation are он HO Select one: O A. i)RCO3H…

A: Hey, since there are multiple questions posted, we will answer first question. If you want any…

Q: What reagents are needed to accomplish the following transformation? CH3 O 1- Hg(OAc)2, H₂O 2-…

A: When an alkene undergoes hydroboration Oxidation Reaction, then an alcohol is formed according to…

Q: 1. Describe the following chemical reactions as SN1, SN2, E1 & E2. Draw a curved arrow mechanism for…

A: The answer is given below

Q: 'hich of the following reagent best accomplish this transformation below? -CH=CH- -CEC- A (1st)Br2,…

Q: What major product will be formed when the shown Grignard reagent is combined with the shown…

A: Given reaction,

Q: Consider the following reagents. A) H30* B) OH- C) CO2 D) Mg/THF E) KCN F) SOCI2 G) NABH4 H) LAH I)…

A: In the field of organic chemistry, Grignard reagents are particularly valuable organometallic…

Q: 4. a. Which of the following would be more reactive in an electrophilic aromatic substitution ?…

A: 4 a. Electron donating groups increases the reactivity of benzene ring towards electrophiles.…

Q: Rank the following alkyl chlorides below in terms of increasing reactivity with a nucleophile via…

Q: Which structure is the best nucleophile for an SN² reaction? A. NH3 B. NH2 C. NH4* D. HCN O B

A: The question is based on the concept of reactive intermediates. We have to identify which is the…

Q: Identify the reagents C in the following scheme: он CH3 CH3 CH3 OCH3 он CH3 CH3 OH O N2OCH3 with…

Q: a. Rank in order of S2 reactivity (1= most reactive) b. Rank in order of leaving group ability (1=…

Q: Rank the species in each group in order of increasing nucleophilicity. a. CH3CH2S−CH3CH2O−, CH3CO2−…

A: Since we only answer upto 3 sub-parts we'll answer the first 3. Please resubmit the question and…

Q: Which nucleophile in each pair which would give the faster SN2 rate? (a) (CH3)2S or (CH3)2Se (b)…

A: SN2 is the Nucleophilic Substitution Bimolecular reaction. The nucleophile that attacks the…

Q: Rank the attached compounds in order of increasing reactivity in asubstitution reaction with −CN as…

A: Nucleophilicity is defined as the tendency to give the electrons. And, a better nucleophile can…

Q: Which of the following SN2 nucleophiles does not lengthen the carbon-carbon chain? KC≡C-C6H5…

Q: Which mechanism involves a carbocation electrophile reacting with a weak nucleophile? Group of…

A: Carbocation - carbon carries positive charge Nucleophile - electron rich species Electrophile -…

Q: In which direction will the following reaction proceed? Forward or Inverse CH3 NH CI N-CH3 CH3 CH3…

A: There are three conditions to predict the direction of a reaction. Q can be used to determine in…

Q: What are the steps to get the answer?

A: In a nucleophilic substitution reaction one nucleophile substitutes the other nucleophile (leaving…

Q: 1. What reagents will accomplish the following multistep synthesis? A) HBr, CH,00CH3 B) HBr C)…

Q: 3. Circle the nucleophile in each pair that undergoes SN2 reaction most rapidly with Ph-CH2-Cl in…

Q: In an SN2 reaction, which of the following nucleophiles will produce an ether? "C=CH "OH "O-C-CH3…

Q: Which reagents would best accomplish this transformation? %3D .C. HO, CH3 CH3 CH3 (A) K,Cr,O, +…

A: The reaction given is,

Q: Which reagent in each of the following pairs is more nucleophilic? a) (CH3)3B and (CH3)3N b) H2O…

A: The reagent has a negative charge or lone pair of electrons acts as a nucleophile. As the…

Q: Which of the following is the least reactive towards a nucleophile? O C A Н3С о A Н Н С O B CH3 C…

Q: Which of the following reactant will not favour nucleophilic substitution reaction ? (a) (b) Ph – Br…

Q: Which is the correct order of reactivity towards a nucleophile, from most reactive to least? H3CO F…

A: Given compounds:

Q: The most reactive compound(s) towards nucleophilic acyl substitution reactions? H3C HO H3C OCH3 H3C…

A: A chemical reaction in which an electron-rich species attacks an electron-deficient carbon atom and…

Q: CH3 CH3 CH3 H-C-CI CH3-C-CI CH3-C-CI H-C-CI H CH3 H NOP QRS TUV WXY HICIH

A: reactivity of SN2 mechanism decreases on increasing the substituent on the carbon attached to…

Q: Arrange the following ketones in order of increasing reactivity towards nucleophiles with the least…

A: The carbonyl compounds give nucleophilic addition reactions. The carbon atom of the carbonyl carbon…

Q: Which of these nucleophiles would be the best for converting a tertiary alkyl halide into an…

A: Nucleophilic substitution is that type of reaction in which electron rich nucleophile attacks the…

Q: Identify the stronger nucleophile in each pair. a. NH3,−NH2 b. CH3NH2, CH3OH c. CH3CO2−, CH3CH2O−

A: Nucleophile : Molecule which easily donates electron pair are called nuclephile.

Q: Which molecule can loose a hydrogen and become a nucleophile? Select one: a. H3C- ECH b. H3C- -CH3…

A: Solution:

Q: Give the major product from A-E Give the major product trom A-E. the HBr D H2O2 H2 A Ni Ch H/H2O E C…

A: Different reagents are used for the synthesis of a compound (product) from the different compounds…

Q: A set of three nucleophilic displacement reactions is shown below: CH3 CH3 CH3Br CH;CHCH2CH2B1…

A: The correct answer about SN2 reaction is given below

Q: Which of the following molecules would react most rapidly in a nucleophilic substiution reaction?…

Q: Which of the following is the best nucleophile in an SN2 reaction? Group of answer choices H2O…

A: Nucleophile: electron-rich molecules are called nucleophiles. Here, the given nucleophile: H2O…

Q: Predict the major product A-E. cold dilute KMnO4 A Ch H2 Ni O3 uv Zn/CH3COOH hot KMNO4 ОН H30

Q: Rank the compounds in each group in order of increasing reactivity towards nucleophilic addition a)…

A: An electrophile is a carbon species that might be neutral or positively charged. Similarly, a…

Q: CH31 Na Rate=k[substrate][nucleophile] ОН Br "Br H20

Q: A set of three nucleophilic displacement reactions is shown below: CH3 CH3 CH,CHCH,CH,CCH,CI CH3 CH3…

A: tertiary alkyl halide tends to undergo the SN1 faster than secondary or primary alkyl halide because…

Q: What reagents (A-D) are needed to carry out each reaction in the following sequence? A в O2N `SO3H…

A: Reagent is a compound which is added to a system to cause a chemical reaction, or added to test if…

Q: Which compound undergoes the fastest nucleophilic acyl substitution? A. B. H3C D. С. O,N O,N NO

A: In nucleophilic acyl substitution reaction, a nucleophile attacks the C atom of -C=O and removes the…

Q: Which is the least reactive towards nucleophilic acyl substitution? a) H₂C-C-Cl c) H₂C-C-NH₂ 1₂C-E-N…

A: Reactivity of the carbonyl compound depends on the electrophilicity of (C=O) and the leaving…

Q: Which reacts the most rapidly in a nucleophilic substiution reaction? a. 2-Iodo-2-methylpropane…

A: The substitution of an incoming nucleophile in an organic compound is called nucleophile…

Concept explainers

Alkanes and Cycloalkanes

Alkanes are saturated organic compounds which are made up of C and H atoms. Alkanes have the general formula of CnH2n+2. Alkane contains sp3 hybridized carbon atoms with four sigmas (σ) bonds & every hydrogen atom is connected with one of the carbon atoms. The size of the alkane could be determined by the number of carbon atoms located in it.

Question

Give the organic product:
H-S-CH,CH3
(HINT: "S" is a nucleophile )
S-CH,CH3
-S-CH2CH3
A
ОН
S-CH2CH3
B
D
НО
CH3CH2-S
Select one:
В
A

Expert Solution

This question has been solved!

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

SEE SOLUTION Check out a sample Q&A here

Step 1

VIEW

Step 2

VIEW

Step by step

Solved in 2 steps with 1 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

In the synthesis of 2-methyl-pentan-2-ol from pentan-2-one, the source of the nucleophile in nucleophilic attack on the carbonyl carbon is __________. -C≡N CH3MgBr -C≡CCH3 NaOCH3 KMnO4
Brevicomin, the aggregation pheromone of the western pine bark beetle, contains a bicyclic bridged ring system and is prepared by the acid-catalyzed cyclization of 6,7-dihydroxynonan- 2-one. a. Suggest a structure for brevicomin. b. Devise a synthesis of 6,7-dihydroxynonan-2-one from 6-bromohexan-2-one. You may also use three-carbon alcohols and any required organic or inorganic reagents.
Explain the following observation. Ethyl 3-phenylpropanoate (C6H5CH2CH2CO2CH2CH3) reacts with electrophiles to afford ortho- and para-disubstituted arenes, but ethyl 3-phenylprop-2-enoate (C6H5CH= CHCO2CH2CH3) reacts with electrophiles to afford meta-disubstituted arenes.
Brevicomin, the aggregation pheromone of the western pine bark beetle, contains a bicyclic bridged ring system and is prepared by the acidcatalyzed cyclization of 6,7-dihydroxy-nonan-2-one. a. Suggest a structure for brevicomin. b. Devise a synthesis of 6,7-dihydroxynonan-2-one from 6-bromohexan-2- one. You may also use three-carbon alcohols and any required organic or inorganic reagents.
Treatment of compound A (C8H17Br) with NaOCH2CH3 affords two constitutional isomers B and C. Ozonolysis of B affords CH2=O and (CH3CH2CH2)2C=O. Ozonolysis of C affords CH3CH2CH2COCH3 and CH3CH2CHO. What is the structure of A?
Write the structure of the compound E,E-2,4-Hexadien-1-ol and label each non-equivalent carbon with a letter, A,B,C..
Give the major products or reagents represented by letters E and F:
1.Describe the ozonolysis of alkenes 2.one mole of a hydrocarbon(A) reacts with one mole of beomine giving a dibromo compound C5H10Br2.Substance A on treatment with cold dilute kMnO4 solution forms a compound C5C12O2(C5H12O2) on ozonolysis A,gives equimolar quantities of propanone and ethanol.Deduce the structure of substance A.
Explain this observation: Ethyl 3-phenylpropanoate (C6H5CH2CH2CO2CH2CH3) reacts with electrophiles to afford ortho- and para-disubstituted arenes, but ethyl 3-phenylprop-2-enoate (C6H5CH=CHCO2CH2CH3) reacts with electrophiles to afford meta- disubstituted arenes.
Deduce the structure of each compound from the information given. All unknowns in this problem have molecularformula C8H12.(a) Upon catalytic hydrogenation, unknown W gives cyclooctane. Ozonolysis of W, followed by reduction with dimethylsulfide, gives octanedioic acid, HOOC¬(CH2)6¬COOH. Draw the structure of W.(b) Upon catalytic hydrogenation, unknown X gives cyclooctane. Ozonolysis of X, followed by reduction with dimethylsulfide, gives two equivalents of butanedial, O“CH¬CH2CH2¬CH“O. Draw the structure of X.(c) Upon catalytic hydrogenation, unknown Y gives cyclooctane. Ozonolysis of Y, followed by reduction with dimethylsulfide, gives a three-carbon dialdehyde and a five-carbon dialdehyde. Draw the structure of Y.*(d) Upon catalytic hydrogenation, unknown Z gives cis-bicyclo[4.2.0]octane. Ozonolysis of Z, followed by reductionwith dimethyl sulfide, gives a cyclobutane with a three-carbon aldehyde (¬CH2¬CH2¬CHO) group on C1 and aone-carbon aldehyde (¬CHO) group on C2. Draw the…
Oximene and myrcene, two hydrocarbons isolated from alfalfa that have the molecular formula C10H16, both yield 2,6- dimethyloctane when treated with H2 and a Pd catalyst. Ozonolysis of oximene forms (CH3)2C = O, CH2 = O, CH2(CHO)2, and CH3COCHO. Ozonolysis of myrcene yields (CH3)2C = O, CH2 = O, (two equiv), and HCOCH2CH2COCHO. Identify the structures of oximene and myrcene.
Compound A (C7H11Br) is treated with magnesium in ether to give B (C7H11MgBr), which reacts violently with D2O togive 1-methylcyclohexene with a deuterium atom on the methyl group (C). Reaction of B with acetone (CH3COCH3)followed by hydrolysis gives D (C10H18O). Heating D with concentrated H2SO4 gives E (C10H16), which decolorizestwo equivalents of Br2 to give F (C10H16Br4). E undergoes hydrogenation with excess H2 and a Pt catalyst to giveisobutylcyclohexane. Determine the structures of compounds A through F, and show your reasoning throughout