Design a two step synthesis that converts 3-pentanone into 3'-pentyl acetate as shown below.CH3H2CH2H2C.ACH3„CH3H3CHH2Draw the structure of molecule B and write the reagents A and C for the two steps in the multi-step synthesis.

we can convert one functional group to another by various reaction pathway like substitution or…

Design a two step synthesis that converts 3-pentanone into 3'-pentyl acetate as shown below. H2 -CH3 H2 CH3 CH3 H3C H2 Draw the structure of molecule B and write the reagents A and C for the two steps in the multi-step synthesis.

Design a two step synthesis that converts 3-pentanone into 3'-pentyl acetate as shown below. H2 -CH3 H2 CH3 CH3 H3C H2 Draw the structure of molecule B and write the reagents A and C for the two steps in the multi-step synthesis.

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

Chapter6: Reactions Of Alkenes

Section: Chapter Questions

Problem 6.15P

See similar textbooks

Related questions

Q: Draw structures for the carbonyl electrophile and enolate nucleophile that react to give the aldol…

A: The carbonyl electrophile and enolate nucleophile both are present in a single compound

Q: Without changing reagent concentrations or amounts, what change could one make to the reaction shown…

A: Given reaction is Nucleophilic substitution reaction of 1o (primary) alkyl bromide , which is more…

Q: Use retrosynthetic analysis to plan a synthesis of the following target molecules. The only…

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

Q: Draw structural formulas for the alkoxide lon and the alkyl(aryl)bromide that may be used in a…

A: Alkyl bromide reacts with alcohol to form an ether by the Williamson ether synthesis. The reaction…

Q: Complete each of the following statements below using the figure below. NaOH a. In the above…

A: Nucleophile is negatively charged or neutral species. Electrophile is positively charged or neutral…

Q: Use retrosynthetic analysis to show how hex-3-yne can be prepared from acetylene and any other…

A: Hex-3-yne can be synthesized from acetylene using suitable reagents. This can be shown using…

Q: Perform a retrosynthetic analysis and suggest a synthesis of the target molecule (on the left) from…

A: The Retrosynthesis method is the method that determines the starting material by the fragmentation…

Q: Starting with 2, 9- decanediol, design a synthesis for 3-hydory-3- Methylcyclononanore.

Q: Design multiple step synthetic routes to prepare the target compounds from the starting materials.…

A: This question belongs to multistep organic synthesis. Find the complete solution given below

Q: Show the reaction between 1-bromopentane and sodium ethoxide using curved arrows.

Q: NCH, Starting with the Claison reaction of ethyl acetate and itself. Use any other reactants with 3…

A: Claisen Condensation: The Claisen Condensation, which is assisted by a base such as sodium ethoxide,…

Q: 4. Write in the reagents need to transform benzene into this product. Benzene ->

Q: 2. In a Williamson Ether Synthesis of Phenacetin When the reaction is complete, water will be added…

A: In the synthesis of phenacetine sodium acetamido phenolate reacts with ethyl bromide to form the…

Q: Draw structures for the carbonyl electrophile and enolate nucleophile that react to give the enone…

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

Q: Write a detailed, stepwise mechanism for the following reaction. CH3 Cl2 -CH2CI + HC1

A: The structure in which the electrons are delocalized on the three or more atoms which cannot be…

Q: d) .F

A: benzene undergoes electrophilic substitution reaction due to pi-electron cloud over the whole…

Q: Write structures for the carbonyl electrophile and enolate nucleophile that react to give the aldol…

A: Aldehydes or ketones having atleast one alpha hydrogen atom when treated with dilute base undergo…

Q: turbo-Grignard reaction, please tell me the reason for reacting 2-chloropropane first. After that,…

A: The Grignard reagent is expressed as RMgX, Where R can be an alkyl or aryl group and X is a halogen…

Q: Draw the alkyl bromide(s) you would use in a malonic ester synthesis of ethyl…

A: The required alkyl bromide is 1,4 dibromobutane.

Q: Compounds A, B, and C which are all alcohols are subjected to the Lucas test. An oily layer was…

Q: Draw structures for the carbonyl electrophile and enolate nucleophile that react to give the enone…

A: A carbonyl electrophile and an enolate (formed after the deprotonation of an aldehyde/ketone)…

Q: Identify the reagents reeded for the two Step Synthesis below; Ph Step1! Step2

A: An organic chemistry based question, which is to be accomplished.

Q: Show the arrow pushing mechanism for getting tropylium ion from the benzylic carbocation

A: In the given question we have to rearrange the benzylic carbocation to tropylium ion.

Q: Br-

A: Note: Olefin undergoes electrophlic addition reaction. But the cyclobromonium ion is opened by…

Q: write reagents of this reaction

Q: Draw the structure of the starting material in this hydration experiment.

A: This experiment is synthesis of hexan-1-ol by hydration of hex-1-ene.

Q: Suggest a synthesis for the molecule shown below. Only starting materials containing six (6) carbons…

A: The key reactions involved in the synthesis of given target material are: 1) Friedel-Crafts…

Q: 2. For the reaction scheme below: (i) Suggest a reagent X that could be used to accomplish the first…

Q: a. Can you predict an undesirable side reaction that might occur using ethanol as a solvent that…

A: Carbocations are electron-deficient species that are produced from a substrate by the removal of the…

Q: how would you deconstructing” a target molecule into its readily available, simple starting…

A: This synthesis involves Michael addition, aldol condensation, hydrolysis and decarboxylation

Q: What is the IUPAC nomenclature of the main product formed during this mechanism?

A: 4 bromo octane will be the major product in this reaction as it is formed through a more stable…

Q: Below are several common solvents in organic chemistry. Select those that would not be compatible…

A: Given : structure of molecules Grignard does not react with ether, alakne, benzene

Q: Evaluate the chemical reactions carefully. Predict the reagents required (marked with letters) in…

A: Given : structure of reactant and product.

Q: a. Mix 1 mL of glacial acetic acid, 1 mL of ethyl alcohol and 3 drops of concentrated sulfuric acid…

Q: Please complete the following conversion and show work in mechanisms. Name the final product and…

Q: Br bromobenzene 1-phenylpropan-1-one

Q: b) Describe the steps involved in the synthesis and the role of each step. Each step should clearly…

Q: Draw structural formulas for an aldehyde or ketone and alkyl (or aryl) bromide that could be used in…

A: Alkyl magnesium halide is known as a Grignard reagent. The general formula of the Grignard reagent…

Q: 5. Briefly explain your answer to the previous question in terms of the merits or drawbacks of each…

A: The suitable reagent for the conversion of R(CO)Cl to R(CO)CH3, (CH3)2CuLi is used.

Q: Enolates are formed by deprotonation of an α-carbon hydrogen. Answer the following questions about…

A: in this given molecule alpha carbon is adjacent carbon of carbonyl group, that is at the ring…

Q: OH Reaction 1 Reaction 2

Q: The compound below can be prepared with an alkyl iodide and a suitable nucleophile. Identify the…

A: The given structure of the compound appears as follows: The structural formula of the above…

Q: Draw structural formulas for the α,β-unsaturated aldehyde or ketone and the lithium diorganocuprate…

A: Given compound has a cyclopentanone ring as skeleton. When alpha,beta-unsaturated aldehyde or…

Q: The SN2 reaction can be carried out intramolecularly (in the same molecule). What product do you…

Q: Write structures for the carbonyl electrophile and enolate nucleophile that react to give the aldol…

Q: Why is the reaction of the type shown below usually done? a.To make an aldehyde or ketone less…

A: We've to predict the function of the reagent in the given reaction.

Q: Complete these reactions involving lithium diorganocopper (Gilman) reagents

A: Gilman reagent The reagent which has the form R2CuLi, where R is alkyl group. In the reaction,…

Q: Draw structures for the carbonyl electrophile and enolate nucleophile that react to give the enone…

A: Aldol condensation: The alpha hydrogen of carbonyl compounds is acidic in nature and it is removed…

Q: 1.) Why are functional group interconversions controversial? (double bonds into epoxide) 2.) Explain…

A: A double bond (alkene) converts into an epoxides as : Functional group modification or…

Question

Design a two step synthesis that converts 3-pentanone into 3'-pentyl acetate as shown below.
CH3
H2C
H2
H2
C.
A
CH3
„CH3
H3C
H
H2
Draw the structure of molecule B and write the reagents A and C for the two steps in the multi-step synthesis.

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

Protection of Groups in Organic Synthesis

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

X Upon ozonolysis, Compound X produces two compounds: Compound Y and Compound Z. Compound Y can also be prepared from the following synthetic route: PCC 1. R₂BH, THF 1. Mg. Et₂O PCC Compound Y 2. CH₂Cl₂ 2. NaOH, HO CH₂Cl₂ 3. H₂O* From this information, draw the structures of Compounds X, Y, and Z. For Compounds X and Z, different substituents are possible. For grading purposes, just use hydrogens as the substituents. Br مرد →] ►
1-lodopropane reacts with sodium ethoxide to give: Select one: O a. CH;CH,0CH¿CH2CH3 O b. CH3CH20CH2CH3 Oc. CH;CH20CH3 O d. CH30CH2CH2CH3 The set of reagents (and condition) that would give the best yield for ethyl isopropyl ether is Select one: O a. CH3CH2ONA, (CH3)2CHBr O b. CH3CH2OH, (CH3)2CHOH, H2SO4, 140 °C O c. (CH3)2CHONA, CH;CH,Br Od. CH3CH2ONA, (CH3)2CHOH
7. Provide intermediate products and the final major product for the following reactions: 2-butyne reacts first with (a) Li/NH,(1), -78°C, then (b) HBr, and (c) OH/heat.
By means of a series of equations outline a method for carrying out the ff. conversions. You may use reagents you wish. More than one step maybe required. a. acetylene b. cyclohexanone c. ethyl bromide d. benzene athanol +methylcyclohexanol acetaldehyde +phenyl ethanol B-ethyl-3-pentanol tyclopentanone 2-суano-2-pentanol benzyl alcohol 2-butanone-semicarbazone е. 3-рentanol f. cyclopentene g. 2-pentanol h. benzene i. 2-butanol
Which set of reagents would be appropriate to synthesize bromobenzene from benzene? 1. HNO3 in H2SO4; 2. H2Cr04 and heat 1. H2CrO4 and heat; 2. H2 Pd/C Br2 and FeBr3 1. CH3CH2CHCI and AICI3; 2. H204 and heat 4B12 and Fe Heat and Br2 Br2, HCI
2. The reaction of 2-bromo-2-methylbutane with sodium ethoxide at 50 °C leads to the formation of 2-methyl-2-butene.
S.10. Describe the product formed as a result of the reaction between cyclohexanone and 3-butene-2-one by also writing the mechanism of the reaction. 1'CH,ON H;C, 2 HO CH,
Convert 2-pentanol into 2,3-dibromopentane. Draw structures of the starting material (2-pentanol) and final product (2,3-dibromopentane), and show the two reactions needed for this synthesis. Include the structure of the intermediate compound, and the reagents and conditions for each reaction. Then explain why 1,2-dibromopentane would not be a significant product of this synthesis.
1. Write organic products of the following reactions. Show stereochemistry where appropriate. Br₂ H₂O H₂O H₂SO4 1. BH3: THF 2. H₂O2, NaOH
g) Arrange the following acylating reagents in terms of increasing reactivity. Discuss your choices. `NH -NO 2 `NH `NH. i ii i h) Arrange the following acylating reagents in terms of decreasing reactivity. Discuss you choices comprehensively. H3C O. F3C H3C (а) (b) (c) i) Which strategy is used in the following reaction to prevent alcohol formation? Motivate. OCH 3 Na H2C- (after H 0*workup)
Write the Ky reactions for pyridine, for sodium 2-mercaptoethanol, and for cyanide. H+ binds to S in sodium 2-mercaptoethanol and to C in cyanide. (Hint: Spectator ions, which do not react in solution, appear on both sides of the reaction and can be removed.) N: HOCH.CHS: Na+ CN Pyridine Sodium 2-mercaptoethanol Cyanide Refer to the Ka values below for their conjugate acids. Which of the three bases shown above is the strongest? NH HOCH.CH.SH HCN Pyridinium ion K. = 6.3 x 10-6 2-Mercaptoethanol K. = 1.9 X 10-10 Hydrogen cyanide K = 6.2 x 10-10
Write/illustrate the detailed reaction mechanisms for the following transformations: 1. Synthesis of 1-bromooctane from 1-octanol 2. Synthesis of 1-pentene from 1-pentanol