Presented 4 target molecules, A. Disconnect the target molecule so that a simple starting compoundcan be obtained B. Write down the possible synthesis reactions and the required reaction conditions Please Answer max in 30-40 minutes thank u so please

Q: For the reaction shown below, draw the structure(s) of the major product(s) expected. Do not draw…

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Q: Draw the products of attached reaction.

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Q: CHCI3, t-BuOK

A: The reaction of 1-methylcyclopentene with CHCl3 and t-BuOK gives syn addition product and the…

Q: or the reactions belowW, draw out the reactions as shown and ansSwer the following questions fo ach…

A: The details solution for this is provided below in attach image.

Q: ion was found to E he reaction rate to fo

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Q: 4 Design the synthe tic route: NOz

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Q: The reaction of 3-methylpent-2-ene A with HCl can lead to two possible regioisomeric products, B and…

A: The solution of the question is given below:

Q: c. Show the mechanism for the initiation and propagation steps using the molecules below. Then show…

A: To provide the mechanism of the initiation and the propagation step of the given polymerization…

Q: the 1-pentyne is reacting with CH3CH2CH2Li, then with the ketone, and lastly with NH4Cl and H2O.…

A: The solution of above question is-

Q: indozolin(i) from CH2COOC2H5 N OH

A: Indozoline is prearped from Chchibabin reaction

Q: Please provide a reasonable mechanism for the following transto the stereochemistry of all…

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Q: Draw the products of attached reaction.

A: The given reaction is Friedel-crafts alkylation reaction. The two substituents on the phenyl group…

Q: Dec els fomebs oa.

A: DCC i.e. dicyclohexylcarbodiamide is used as coupling agent . C=O is more stable over C-O , that is…

Q: HÖ- Apply Mechanism O: Hint Solution 8 remaining step(s) can be solved

A: Carboxylic acid: 2-methyl butanoic acid Catalyst: Concentrated sulfuric acid Alcohol: As the name of…

Q: d) synthesize reaction. please show mechanisms if there is any.

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Q: (a) (i) Using AIBN as the initiator, illustrate the mechanism for this polymerization process. The…

A: Answer - According to the question - Given -  The entire process begins with a molecule known as an…

Q: Sive the complete. mechanism of organic Reaction. 유 th+HoCy excess

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Q: Nitration

A: According to the question, we need to explain why nitration requires us to leave the reaction for no…

Q: synthesized calcitriol in *

A: Here fill in the blank question is  given.

Q: Ph Sens

A: first photochemical reaction occour then hydrolysis occour to form ketone

Q: b) Visualise following instructed) (i) the retrosynthesis for the target compounds (as along with…

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Q: Please show the complete steps as well as arrowing pushing mechanisms for the following reaction.

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Q: Explain why the reverse reaction ?? ← ? + ? can be neglected. Plot the dependence of the reaction…

A: A question based on kinetics of reactions in solution that is to be accomplished.

Q: of indiante which is the main product. Justify your answer. 6) present the possible mechanism for…

A: To answer: Indicate which is the main product. Justify your answer. Present the possible mechanism…

Q: NaOH (d) * include stereochemistry

A: An organic compound in which a halogen atom and hydroxide group are attached to adjacent carbon…

Q: In the monochlorination ethane, amount 2-chloro bu tone form. Prapose to a small mechanism explain…

A: Halogenation of alkanes proceeds by the free radical substitution reaction. The steps involved are…

Q: what is the mechanism of p-nitroaniline  ??

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Q: d- ナ ease araw the mech a n LS amw the mechanism at &

A: Hello. Since your question has multiple sub-parts, we will solve the first three sub-parts for you.…

Q: Given the information below, write out a reasonable mechanism for the reaction. Where not provided,…

A: Since, change in concentration of KI does not have any effect on rate of reaction, so, it is SN1…

Q: Br t - DuOK Me DM SO

A: The base will abstract the proton and causes ring opening.

Q: for geherating compand exclusive major praduct out line a synthesis ma as the using Compounds Fan G.…

A: Given

Q: What is the product from the sequenceoreactions depicted below?

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Q: cl CHO KOH

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Q: HCI (b)

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Q: Show the retrosinthesis and the conditions for the following reaction. ->

A: Detail mechanistic pathway is given below along with retrosynthetic pathway

Q: онон CHI H* но OH Et;N EIOH Meo OMe Meo OMe Meo OMe Meo- Meo OMe A Meo- OMe mOEt OMe Eto OEt EIo OEt…

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Q: Eom form a synthetic pathway 6or tanget molecule Stauting mateuials must a maximum of 6 Carbons and…

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Q: Synthesize attached product from the given starting materials using an organocuprate coupling…

A: Product from the given starting materials using an organocuprate coupling reaction has to be given.

Q: is increased..... lod before crystallization begins... ...

A: False

Q: Complete the equation by predicting the major product formed in the reaction. Note that the reaction…

A: The given equation is,

Q: Suggest a suitable and possible synthetic method to design the following organic compounds. H3C. А.

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Q: (a) What is umpolung? for Write the mechanism synthesis from the of 1-acetyl-2-cyclohexen-1-ol…

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Q: S) Prndea nablemechanism for tre reaction Hices?

A: Cleavage of ether in presence of HI.

Q: 1 Write a reaction mechanism for the following conversion, including reagents and/or conditions.…

A: Detail mechanistic pathway is given below to carry out the conversion

Q: A student wanted to dry some diacetone alcohol and allowed it to stand over anhydrouspotassium…

A: In the given reaction the compound was diacetone alcohol which when kept with anhydrous potassium…

Q: //sduu Questio Draw the products of the two step reaction sequence shown below. Ignore inorganic…

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Q: OEt HO H. carry our ietrosynthesis of T. Analysis Must be aretrosyntheticioute snowing cne…

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Q: Give the synthesis mechanism for following molecule from methane, ethane or benzene. give clear…

A: Here we have to synthesize the target compound from starting material benzene or methane and ethane…