At which position in the final product is there an ethyl attached?

Q: CH3CO3H

A: In presence of per acid ,ketone molecule undergo Baeyer villiger rearrangement. Among two alkyl…

Q: The by-product of the aldol reaction has not been drawn in this diagram. What is it?

A: Water is the by product in aldol condensation reaction.

Q: Provide the mechanism for the 1st reaction in this synthesis: ВНЗ/ТHF

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Q: Complete the reaction by identifying the major product/s of the reaction:

A:

Q: Complete the mechanism below with the missing structure and arrows. Also identify any acids, bases,…

A: Electrophile is a substance which carry positive charge and nucleophile is a substance which carry…

Q: What would be the major product if they are reacted with the reagents in the second column?

A: Since, you have asked multiple subparts questions, we will solve the first three subparts questions…

Q: NO2 Br

A: The conversion is given below in pic.

Q: Give the major organic product(s) for each step of the following reaction sequence

A: Given, to draw the major product of the following reaction:

Q: Supply the structures of reactant(s) or product(s) for the following aldol and Claisen reactions

A:

Q: Provide the mechanism for the 1st reaction in this synthesis: КОН

A: We have to draw the mechanism of given reaction

Q: The by-product of the aldol reaction is not drawn here, what is it?

A:

Q: Draw curved arrows to show the movement of electrons in this step of the mechanism.

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Q: Draw the curved mechanism arrows that show the deprotonation of phenol by NaOH and draw the major…

A: This the acid base reaction where NaOH act as  strong base and Phenol acts as a slightly milder…

Q: Copy the given reactions and supply curved arrows to account for the formation of the products.

A:

Q: What nucleophile is needed to convert (CH3)2CHCH2CH2Br to attached product?

A: The reaction and the nucleophile required is as mentioned below:

Q: Draw the curved mechanism arrows that show the SN2 reaction of phenoxide with chloroethane and draw…

A: SN2 is bimolecular substitution reaction , which occurs in a single step and in this case no…

Q: Show the full mechanism for the following reaction.

A:

Q: Provide a possible mechanism for this step.

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Q: Rxn E кон

A: Cycloalkyl reactant whose elimination and substitution products are to be determined.

Q: Please solve for the following Stretter Reaction showing the steps and the final product.

A:

Q: NaOEt ELOH, heat

A: -> NaOEt is base which can abstract most acidic hydrogen and generate nucleophile. ->Then…

Q: What is the appropriate electrophile nucleophile and solvent to achieve this final product

A:

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

A:

Q: Predict the product of the following substitution reaction?

A: Nucleophilic substitution biomolecular reaction (SN2): The bimolecular nucleophilic substitution…

Q: Topose a synthesis of the aldehyde using ethane and propane as your only sources of carbon atoms.…

A: Since you have posted multiple questions in a session, as per guidelines we are entitled to answer…

Q: What

A: We will write the final product of the reaction

Q: what one compound would I use as a starting point for the attached reaction?

A:

Q: エース z-z L H H + CH Anything you need け。

A: Detail mechanistic pathway is given below

Q: Show a detailed mechanism (using arrows) for the nucleophilic substitution reaction that would take…

A: Show a detailed mechanism (using arrows) for the nucleophilic substitution reaction that would take…

Q: NH2 Br 1

A: In the given chemical reaction the amino group attached with the benzene ring is replaced by the…

Q: This reaction takes place via a pinacol rearrangement. Draw curved arrows to show the movement of…

A: Sulphuric acid(H2SO4) is used as dehydrating agent which rearranged ketones and also side products…

Q: Please write the mechanism for the following reaction.

A:

Q: What is a multi-step synthesis for the following:

A: The final product can be prepared in the following steps:Step 1 : Preparation of alkene from alkyl…

Q: down the product

A: Given:

Q: Construct a three-step synthesis of 3-bromo-3-methyl-2-butanol from 2-methyl-2-butene by dragging…

A: Step-1 : 3-bromo-2-methylbutan-2-ol formation Step-2 : Epoxide formation Step-3 :…

Q: Draw the major product of this reaction. Ignore inorganic byproducts. Assume that the water side…

A:

Q: Fill in the appropriate reagent or starting material in each of the attached reaction.

A:

Q: Perform a retrosynthetic analysis (please include - disconnection etc) and suggest a synthesis of…

A: The retrosynthesis method is used to determine the starting material by the fragmentation of the…

Q: From each pair, select the stronger nucleophile. Q.)Cl2 or I2 in methanol

A: Given: Cl- and I- in methanol.

Q: Can someone help me with these and explain how they did it? The question is to predict the major…

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Q: Circle the most acidic position in each molecule that could be deprotonated to give an enolate.

A: Enolate is an organic anion generated by the deprotonation of carbonyl compounds. Enols are a…

Q: Please provide a mechanism with curved arrows for this reaction.

A: Mechanism of Fischer esterification.

Q: 4) Provide a Type 2 reaction and mechanism where a trans product is produced where a ketone is…

A:

Q: What is the complete mechanism for this F!she rxn?

A: When carboxylic acid is treated with alcohol in the presence of mineral acid, generally H2SO4, we…

Q: What is the strongest nucleophile, NH3, CH4, CH3O-, or H2O?

A:

Q: If both size of the ketone and electronics of the aldehyde affect the overall reaction rate, which…

A: In aldol condensation a carbonyl compound forms α,β unsaturated carbonyl compound. In this the…

Q: Can you show step by step of this missing reagent and show the synthetic intermediate?

A: Selective reduction of ester in present of ketone is done by NaBH4. We protect the ketone so that…

Q: CH,0-P-8 OCH, CH;0O, NaOCH3 H. OCH3 + CH,0 OCH3 CH;OH CH;0 CH;0

A: This is an example of Wittig-Horner reaction

Q: a) Show a detailed mechanism for the reaction to produce nitrogen gas and the two carbon radicals…

A: "Since there are multiple sub-parts in this question and it is not mentioned that which one has to…

Q: What is a correct mechanistic step of this reaction?

A: The given reaction is SN2  reaction because the  inversion of stereochemistry of reaction  occurs .…

Designing a Synthesis

Organic synthesis is a branch of chemical synthesis that involves the planned construction of organic compounds/molecules from smaller units that possess functional groups. Friedrich Wöhler was the first scientist who designed the synthesis of an organic compound, urea from inorganic starting materials silver cyanate with ammonium chloride via a simple, one-step synthesis.