what will be the steps involved to yield the product in this reaction

Q: H2O H2SO4

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Q: select the major 1. NaOCH2CH3 CH3CH2OH CH3CH30 OCH2CH3 2. H3o+ OCH2CHS OCH2CH

A: The given reaction is an example of an intramolecular Claisen condensation reaction.

Q: Nal OEt NME2 NaHCO3 ?? ?? 10 °C 25 °C ŅME2 PhMgBr ?? ELOH ?? -78 °C → 25 °C 80 °C

A: For 1,2-addition: i) Nucleophile should be strong, ii) Reaction at low temperature.    For…

Q: HgSO4/H₂SO4/H₂O NaBH4 MeOH 1.) NaH 2.) CH3CH₂Br

A: When terminal alkyne is treated with mercury and sulphuric acid then ketone is formed .The reduction…

Q: Curved arrows are used to illustrate the flow of electrons. Using the provided starting and product…

A: The Bronsted-Lowry acid-base theory states that the acid is a substance that gives H+ ions and the…

Q: reaction

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Q: Startng product wait oan

A: Dehydration of alcohol takes place in presence of dilute sulfuric acid. Initially oxygen of alcohol…

Q: What are the major and minor products of this reaction

A: The major product can be obtained by E2 pathway and the minor product can be obtained through SN2…

Q: What is the final product of the following synthesis? Н2 i. OsO4 Ni2B (P-2) ii. NaHSO4 HO Н Ш ОТ ФII…

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Q: Determine the reagents that would yield the product. Show the intermediates. OH Br

A: Here we are required to find the reagent needed for conversion of ethyl benzene to desired product

Q: Br 1. Mg. 2. CO₂, then H3O* 3. Methanol, H*

A: When benzyl bromide is treated Mg powder forms a Grignard reagent. Benzyl magnesium bromide when…

Q: HBr A NaCN В HCI/H2O SOCII2 E H2O2

A: General organic transformation

Q: 3. Draw the product to the following reactions. а. .CI AICI3 b. HNO3 H2SO4 C. Br H2SO4 heat d. NO2…

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Q: What product would you expect from the reaction below? H₂C-Br KO

A: A strong base can also acts as a nucleophile. The given tertiary butyl alcohol(KOC(CH3)3) is a bulk…

Q: Consider the reaction coordinate diagram for the reaction below. How many steps is this reaction?…

A: The progress of a reaction can be represented by the reaction coordinate diagram. In a reaction…

Q: Provide the product or reagent that completes the reactions

A: NOTE: please note according to our policy , we can only answer first three subparts of a question.…

Q: H₂O (1) 11 H CH3CH₂CH2N- H (aq) + OH- (aq) 1 CH₂CH3

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Q: How many intermediate/s is/are present in the reaction based from the energy diagram as shown below

A: For a single step reaction no of transition state = 1. Intermediate = 0.  For two steps process, no.…

Q: a. b. Me Me 'Br Brz 2 KOtBu NaNH, Hz (g) CH₂Cl₂ HO-Bu BnBr Lindlar's A DMF cat. Me CH₂P (Ph)3-CPBA…

A: The given problem involves a series of organic reactions using wide variety of organic reagents.

Q: Please provide the product for this reaction.

A: The epoxide ring opening takes place with the Grignard reagent. The nucleophile of the Grignard…

Q: What is the systematic name of the product P of this chemical reaction

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Q: Can you answer this question? Identifying the reaction mechanism

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Q: OMe NaOMe (excess)

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Q: What mechanism would you use or what steps would you take to get from the reactant to the product?

A: Explain the mechanism of the given organic reaction

Q: Consider the following overall reaction, which will be discussed in Chapter 20.

A: Reaction of a carbonyl compound and an enolate ion generates beta-hydroxy carbonyl compound,…

Q: Br NaSH DMF

A: In SN2 reaction, we get the inversion form as a product because reaction completes in one step.

Q: predict the product of the given reactions

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Q: H3PO4 Choose all intermediates that are formed during the reaction. Carbocation O Alkoxide Oxonium…

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Q: 1. PhSH D 2. H30' H3C, HBr, Et,O E HBr, H2O F

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Q: QUESTION 17 What conditions are required to complete steps 4 and 5 (i.e., the last two steps) in the…

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Q: pt - Reaction mechanism and curved arrow notation are challenging topics. Arrowheads with two sides…

A: In the given reaction the allylic bromide gets hydrolyzed and forms alcohol and alkene. The reaction…

Q: For the following reactions, complete the reactions by giving what is missing.  This can be either…

A: The conversion of one organic compound into others is done by different types of reaction, all these…

Q: Describe two ways the following reaction can be carried out

A: Wolff Kishner reduction is a reaction to reduce ketones to alkanes. The reagent used to reduce…

Q: Si KF CH3COOOH

A: We know Si-F bond is so strong because of back bonding . -ve charge stability depends on…

Q: Draw the content of the final reaction mixture. Explain your reasoning.

A: Since nitrogen is reacting with hydrogen to form ammonia as per the reaction  N2 (g) + 3 H2…

Q: CH OH PhMgBr

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Q: What is the product of this three step reaction sequence?

A: Here we are required to predict the major product of the reaction.

Q: what is the reaction mechanism for this reaction?

A: Step 1:

Q: What's the mechanism process to get this product

A: ylide formation

Q: Consider the given reaction in which NC−NC− is the nucleophile and CH3CNCH3CN is the solvent. The…

A: The solution is as follows:

Q: Determine the product for each reaction. HBr -FE OCHCH, 6. CH 1) CH,CH,O Na HOW OCH,CH, DCHCH, C H…

A: Epoxide ring opening reaction takes place when treated with nucleophiles. Ring opening reduces the…

Q: 3. Does it matter what order you mix the reactants together in? If so, what is the correct order? 4.…

A: 1) Yes in the reaction, it is very important to take care of the order because every chemical that…

Q: 1.NaH/MDSO/CH3I 2.HNO3/H,SO4 3.Fe/HCI CH3 H3C 'N' NH 4.1.HCCOH/Heat 2.HNO/H2SO4 'N' N.…

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Q: Br Et OH. 70°C

A: Tertiary alkyl bromide forms a tertiary carbocation which then abstracts proton and form alkene (…

Q: write which is the corresponding product or products or the reactant (s) to obtain the product.

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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.