H-CC-CH₂ H Complete the synthesis of disparlure from the shown starting material by providing the necessary reagents in the boxes below. H CH₂ - CH₂ CH₂-CH xy 1 CH3 CH3 O H H ケミミ H disparlure Na C=C-CH₂ CH₂-CH₂ disparlure CH₂-CH 1 CH3 CH3

H-CC-CH₂ H Complete the synthesis of disparlure from the shown starting material by providing the necessary reagents in the boxes below. H CH₂ - CH₂ CH₂-CH xy 1 CH3 CH3 O H H ケミミ H disparlure Na C=C-CH₂ CH₂-CH₂ disparlure CH₂-CH 1 CH3 CH3

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 jor product of the following rencfon? CH-CH OH + excess HBr CH-CH Br CH=CH2 b) CH-CHOH…

Q: Write the appropriate reagents and products for each of the following reactions: HO CH3 HCI (2) ?…

Q: Arrange the following alcohols in order of increasing rate of reaction with the Lucas reagent. OH…

A: We have to arrange the following given alcohols in the order of increasing rate of reaction with the…

Q: What are the organic products formed in each reaction? 11 C - C=C - c -C + Br -> 12 C-c -c -c=C +…

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

Q: 11. Which set of reagents, in the presence of a basic catalyst, could be used to prepare this…

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

Q: Show how the acctached compound can be synthesized from the given starting material:

A: Given:

Q: ce CH3-C=CH 2 Hce CH3-C-CH3 ce

A: In the first step the terminal carbon atom of the alkyne will get protonated by one HCl molecule.…

Q: Choose the correct product of the reaction from the choices provided: HBr (2 mol) H3C-CECH Br Br…

A: Markovnikov's rule: According to this rule when hydrogen halide is added to an unsymmetrical alkyne,…

Q: The reagent is incorrect to produce the product below. True/False

Q: "x= a) CHz-C=C-H C内 EHっTHつてH CH3 b) -->

Q: OCH3 CH30-C-CH2-C-OCH3 + CH2=CH-ĉ-H

Q: Provide the reagents necessary for the following conversion. Br A B s 1. NaBH4/CH3OH 2. CH3CH₂MgBr…

A: Grignard reagent is the source of nucleophile which undergoes nucleophilic addition to carbonyl…

Q: Give the major product for the reaction. 1 CHO CHCH CH,CH CHO excess O CH CH CH-CH CH OH CH CH CH…

Q: What are products of the following reaction? CH-CH HEC-O-CH, CH3+KOH- CH-CH-C-OH + CH3CH,OH…

A: This is the base catalysed ester hydrolysis .

Q: CI 2HCI CH3-CECH CH3-C-CH3 CI

Q: What is the major product of the following reaction? CE, C, C C 1 equivalent CE-CE CE-CE₂ + M…

A: The product will be obtained following Markonikov's rule on unsymmetrical alkyne. Hydrogen and Br…

Q: identify both products A and B in the scheme below. но CI-S-CH3 .. K O'Bu A В

A: Given reaction:

Q: What is the major organic product of the following reaction? Br + (CH₂CH₂CH₂)2CuLi CH₂CH₂CH₂ Br…

A: Lithium organocuprates, R2CuLi is known as Gilman reagent. The Gilman reagent is very selective for…

Q: Synthesize 2,4-dimethylhexan-3-one from four-carbon alcohols

A: The starting material in the synthesis is 4-carbon alcohol. Ketones are generally prepared from…

Q: With how many of the following four methods it is possible to obtain propyl acrylate ?

A: how many of the following four methods it is possible to obtain propyl acrylate.we can find the…

Q: Indicate the reagents for the transformation: hex-3-en-2-one → 3,4-dibromohexan-2-one

Q: H3C, H3C, Br CH3 CH3 H3C H3C Br

Q: ⑤Draw the products for the following reactions. CH 유 -(CH2) 4-CH=CH-CH2-CH=CH-CH2-CH=CH(CHI)y CH3…

Q: CH;CH, -Č-OH + KOH KOH What is a major product of the reaction above? OH CH,CH, C-OH CH;CH, C=0…

Q: What is the product of the reaction shown below? O O CH3- CH2- CH = CH, + H,O H+ о ОН ОН I. СН3 - С…

Q: 0 H NaOH 1-cyclopentylpropan-1-one benzaldehyde

A: A mixed aldol condensation reaction involves the condensation of two different carbonyl compounds to…

Q: What are the reagents required to make the following conversions? OEt ? a) b)

A: The given alkyl halide is cyclopentyl methyl iodide which is a primary alkyl halide. The product…

Q: Her 第

A: H2/Pd is reducing agent.

Q: What is the organic product formed in the following reaction? O i cotts A C6H5-CH=CH-C B i-cat…

A: The reaction is a nucleophilic addition reaction in which nucleophile is added to the beta-carbon of…

Q: What are the products of the following reactions, assuming that one equivalent of each reagent is…

A: The substrate in this reaction is a dialkene ( means contains two double bonds ) and the main…

Q: Show the steps necessary to synthesize 2-methyl-2-hexene by the Wittig reaction starting with an…

A: To synthesize this compound using wittig reaction now we have find out the alkyl halide starting…

Q: ОН O: H3C- H3C- ОН HO ОН

A: The products in the given reaction are obtained by the ozonolysis of given reactant, but-3-ene-1-oic…

Q: Pick the major product when 2-butyne reacts with 2 equivalents of HCI. CH3 CI CH3 CHa CH3 C=C

Q: What is the product in the following reaction? CH3CH₂CH₂C=CCH₂CH₂CH3 O trans-4-octane O octane O…

A: In this question, we will find out the major organic product after the reduction of the triple bond…

Q: show by a series of reactions how you could prepare the following from the given starting compound

A: Synthesis of compounds from the given starting reagents.

Q: What products are obtained from the reaction of the following compound with H2CrO4 + Δ?

A: Introduction: In the given reaction, the alkyl side chain present on the benzene ring get oxidized…

Q: Propose a step-by-step mechanism

Q: Give the major organic product of the following reactions. 6 7 8 9 10 #9 answer NaBH4 2 CH₂OH H* CI…

Q: What is the product of the following reaction? ch10-d2-q4a.jpg R-C=C-R+X2 (1 equiv) A) R-CHX-CHX-R…

Q: What is the major Organic product of the reaction Shown below? H + NH3 |CA CH3CH₂CH=H OH CD…

A: Following half reaction is given -

Q: Give the major product for the following reaction CH₂CH=CH Select one: O CH₂C=CH CHỊCHỊCHÍNH…

Q: What is the enol tautomer of the molecule below?

Q: Show the reagents for the conversion below: OH OCH3 NO2

Q: H3C CH3 KMNO4 CH3

A: The permanganate (KMnO4) oxidation of aromatic side chains, as long as there is at least one…

Concept explainers

Reactions at the Alpha Carbon Atom

The position next to the ketone or aldehyde functional group is termed as alpha position and the reaction which occurs at alpha position is called alpha substitution reaction. In an alpha substitution reaction, the alpha proton atom is substituted by an electrophile by the formation of an enol intermediate or enolate ion intermediate. Most of the carbonyl compounds go through an alpha substitution reaction.

Question

H-CC-CH₂
H
Complete the synthesis of disparlure from the shown starting material by providing the necessary reagents in the
boxes below.
H
CH₂ - CH₂
CH₂-CH
xy
1
CH3
CH3
O
H
H
ケミミ
H
disparlure
Na C=C-CH₂
CH₂-CH₂
disparlure
CH₂-CH
1
CH3
CH3

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 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

Give the reagents that should be used to carry out the following synthesis
Give the major product for each of the following reactions
Describe how the following compound could be synthesized from the given start material. X-X OH
complete the following reactions:
Indicate the appropriate reactants, reagents, or products for the following reactions (show all stereochemistry where necessary): OH D H2 A 1. Hg(OAc)2, CH3OH 2. NaBH4 Pt, C peroxyacid C B
Propose a mechanism from the starting material. CH3 O H. 1-methylcyclohex-1-ene H3C CH3
! 11:50 %0AONO propanoic acid can be prepared from reaction with EtONa, CH3-Br And H3O+, heat / -CO2 diethyl malonate ethyl acetoacetate diethyl acetate ethyl acetate i CH₂ a) CH₂-C-PPh a d b) CH₂-C-P CH₂ CH₂-C-C-CH₂ CH₂ CH₂ CH, CH CH₂ O d) CH₂ CH₂ CH₂ C-Phy CH₂
Which reactions yield the same carboxylic acid? K2Cr,0, CH, CH H,SO4 Mg co2 H30*/H20 -CH,CH,Br diethyl ether KMnO4 H3O*/H20 -CH,CH3 KOH / H,0 K,Cr,07 IV -CH¿OH H,SO4 O ,II, II O ,II, IV O II, III, IV O ,II, IV
What is the missing starting material or product? Show stereochemistry and mechanism as needed.
What is the product of the following reaction? CH3CH₂ CH3- н-о- CH CH2 OCH3 OCH3 H CH CH2- CH₂CH₂ CH CH2 OCH₂CH3 OCH CH3 OCH3 -C-H OCH3 OCH3 с H H OCH3 H OCH3 2 CH3OH H* -CH₂CH3