y-valerolactone + 2 equivalents of methylamine ethanoyl chloride + sodium ethanoate

Q: 2. umm Draw the major product of this reaction. Explain your reasoning. Br₂, H₂O EtOH

A: The objective is to determine the product of the reaction. The addition reaction is the addition of…

Q: Draw the Major Organic product of the following reaction. Do NOT use abbreviations such as Ph. Do…

A: Step 1:The Nucleophile attack to the electrophilic carbon centre. Step 2: Since C=O has high bond…

Q: Complete the following reactions by providing either the reactant(s), product(s) or reagent(s) where…

A: Detail solution is given below

Q: Draw the major product of this reaction. Ignore inorganic byproducts and the alcohol side product.…

A: Given that, the reactions are:

Q: consider this step in a radical reaction: CH3 -? What type of step is this? Check all that apply.…

A: The given reaction is one of the steps of the free radical mechanism. It involves the reaction of…

Q: can you please draw the mechanism for this set of reactions? OH Me. Ph OMe Ph OH A. 1. MeMgBr (1 eq)…

A: This is nucleophilic addition reaction. Carbonyl compound react with grignard reagent to form…

Q: j. ethanal + 2 equivalents of NH3 and catalytic amounts of HCI 5. Predict the major new product (if…

A: Given reactions are the organic reactions includes nucleophilic attack at electrophilic centre which…

Q: A student claims the right-hand side of the reaction in the drawing area below shows the product of…

A: An arrow always depicts from a region of high electron density to low electron density ; that is…

Q: 3. Show the mechanism and any intermediates formed in the following reaction. d A

A: retro-Diels-Alder and Diels-alder

Q: What is the missing reactant in this organic reaction? OH R + H₂ Pd Specifically, in the drawing…

A: Carbonyl compounds can be reduced into alcohols. The aldehyde reduces into primary alcohol and the…

Q: i need the answer quickly

A: Given reaction is an example of nucleophilic addition reaction of carbonyl compound.In this reaction…

Q: 5. Draw a complete, detailed mechanism for the following reaction. The atoms on the starting…

A: An arrow always depicts from a region of high electron density to low electron density ; that is…

Q: help please answer in text form with proper workings and explanation for each and every part and…

A: Step 1: Reactants:2,5-dimethyl-3-bromohexane: This is a secondary alkyl…

Q: What following reagents and solvents/temperatures go above and below the arrows to give us the final…

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Q: For the following problem, supply all organic products. The only mechanism followed for each of the…

A: Nucleophillic substitution reaction is a reactiin in which a weak nucleophile is replaced by a…

Q: Draw the product of the reaction shown below. Ignore inorganic byproducts. cat. H₂SO4 SO3 (1 equiv)…

A: Sulfonation of benzene is a chemical reaction in which a sulfur trioxide molecule (SO3) reacts with…

Q: Draw the major product of this reaction. Ignore inorganic byproducts. OH Zn(Hg) HCI O

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Q: None

A: This synthesis problem demonstrates a multi-step organic reaction sequence to convert…

Q: Click on all the atoms that are EXPLICITLY shown in this molecule that have a positive partial…

A: In the given question we have to identify the atoms that have a partial positive charge.The covalent…

Q: 1. Li, NH3 2. HBr, ROOR, hv 3. NaCN, DMSO

A: Here the substrate molecule undergo Birch reduction followed by anti- markonikov bromination…

Q: Draw the major substitution products you would expect for the reaction shown below. If substitution…

A: The steps involved in SN1 reaction are as follows:1. The first step is the formation of a stable…

Q: One of the steps in the mechanism of the above reaction is shown below. Draw the structure of all of…

A: The objective of the question is to identify the product.

Q: None

A: The image shows a step in a radical reaction where a bromocyclopentane radical reacts with an ethyl…

Q: 6. Predict the product of the following, similar to above but a different nucleophile is used and…

A: As we know that grignard reagent act as nucleophile, that's why it attack on epoxide at less…

Q: None

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Q: The correct answer is D, can you please draw the mechanism for the set of reactions shown? А. 1.…

A: In presence of an acid, the epoxide ring is opened from the more substituted side.  TMSCl is used to…

Q: Tat is the major pro > || sequent of reactions? 1. NaOĚt, EtOH 2. Br 3. NaOH, H₂O 4. H₂SO4, H₂O, A…

A: The objective of this question is to explain the mechanism of given ester molecule. It is four step…

Q: Give detailed mechanism Solution with explanation needed. Don't give Handwritten answer

A: The mechanism for this reaction is SN​1 because the carbon atom bearing the leaving group is a…

Q: d. ethyl propanoate + xs NaBH4, later followed by acid e. butanal + 2 equivalents of ethanamine and…

A:

Q: For the following multistep synthesis of the target structure on right from the starting structure…

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Q: Suggest how you would carry out each of these syntheses

A: The given compounds can be synthesized as follows: 1)

Q: (continued) Complete the following reactions by providing the proper substitution AND the proper…

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Q: 10. Each reaction below is missing the substrate, reactant(s), or product(s). () Write the missing…

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

Q: 1. H₂, Pd/CaCO3, quinoline 2a. Hg(OAc)2, H₂O 2b. NaBH4, NaOH

A: The question is based on the concept of organic reactions. we need to identify the intermediate and…

Q: For the following multistep synthesis of the target structure on right from the starting structure…

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Q: Draw the starting alkyne that would lead to this major product under these conditions. Drawing HBr…

A: When alkyne reacts with excess HBr it produce geminal  dihalide .Hence, substrate must be Alkyne .

Q: o O tt. AILLS Ⓒ 2n (Hg) HCl * актион Naor ⒸH3 HOH

A: The above reaction is based on organic reaction mechanism. In the first step of the reaction, first…

Q: Give the major product(s) of the following reaction. HO ? heat

A: Given reaction:

Q: Identify the reagents needed for each step in this synthetic sequence. A ) NaNH2 H 'H C B Na(s) in…

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Q: IOH OH Step 1 Br2, hv КMnOд, NaOH Br Step 3 МеОН, һeat Step 2 .....!"

A: Reactions along with replaced reagents are written below.

Q: Curved arrows are used to illustrate the flow of electrons. Follow the arrows to predict the…

A:

Q: 3. Provide full mechanism (curved arrows and intermediates) for the following reaction. OCH3 1.…

A: Answer 3 )  The mechanism for the given reaction = ?  Note : As per our company guidelines, we are…

Q: Examine the following reaction mechanisms and classify the role of each labeled species in the table…

A: Nucleophile is a species which is electron rich. It has having negative charge or lone pair of…

Q: NH2 same molecular formula will be formed. Briefly (i) explain why this compound cannot be isolated…

A: Solution:The class of given compound is enamine in more correct primary enamine. We know primary…

Q: Consider this step in a radical reaction: Br .CH3 ? What type of step is this? Check all that apply.…

A: The given reaction involves the reaction of a methyl-free radical with a 2-bromo-2-methyl butane…

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.