which is the product obtained from the following sequence of reactions

Q: 1) LAH 2) H3O*

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Q: Но + bas H.

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Q: BV Na O

A: Here in presence of sodium ethoxide as a base acid base reaction via E2 mechanism takes place . For…

Q: О3, -78 Celcius

A: 1) The reaction with Ozone is basically the ozonolysis reaction in which the double bond is broken…

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

A:

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: ОН ОН ох ОН H3PO4 (cat) Д HCI H₂SO4 (cat) Д

A: The first and third reaction are elimination reaction.As here acid condition is given so reaction…

Q: OH H. H3CO OH CH3CO H NH2 HO,

A: The final product is

Q: Draw the structure of the reactant that produces the molecules shown for each of the following…

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Q: Average Exposure to Radiation from Common Sources Source Dose (mrem/year) Naturally Occurring…

A: The data given is,

Q: Mg Br Et20 H30* +

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Q: AIC13 D. A and C E.B and C A C

A: The given reaction is an example of friedel craft reaction.It is an aromatic electrophilic…

Q: Br

A:

Q: OH PBr Mg, Et,Q H,O* heat

A: Given,

Q: Explain why two substitution products are formed in the following reaction.

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Q: H2 Lindlar's catalyst Both A and C A. С. D. B.

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Q: CH3 2) 3)

A: In this reaction we find the correct order of reagents that have to be used for the conversion of…

Q: Give the major products for the reactions

A:

Q: What is the product and the reaction mechanism of the following reaction?

A: To determine the product and reaction mechanism for the given reaction:Please note the second…

Q: is the indicated carbon electrophilic or nucleophilic

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Q: O-H + NAOH eloriools ons oibios alonert

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Q: predict the product of the given reactions

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Q: ŞLi +?→Be + dn }C1 + ?→ 1s + 3He Be + He →3 He + ? BBr + }H -→ ? + 2 3n

A: The nuclear reactions given are Li36 + ?→Be47 + n01Cl1735 + ?→S1632 + He24Be49 + He24 →3 He24 +…

Q: H₂CO CH3 Дон . H2SO. 2) NazCrzO, H2SO., heat

A: First reaction are a Friedel Craft reactionSecond reaction are a oxidation reaction in which…

Q: CeHgLi

A: Introduction :  We have to tell the product for this reaction .

Q: CH3 H, H,O 工

A: A question based on acid catalyzed hydration of alkenes, which is to be accomplished.

Q: ↓ Draw the major elimination products of this E1 reaction. Ignore any inorganic byproducts. E +…

A: E1 reaction is the elimination unimolecular, weak base is used and polar protic solvent is used.

Q: H3C KCN H3C

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Q: A) Alpha Decay of U: B) Beta Decay of “Co: C) Positron Emission of "F: D) Electron Capture of Kr: E)…

A:

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

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Q: ян О. но C=C

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Q: Explain why two substitution products are formed in the attached reaction.

A: Given,  Reactant 1 = 2-Chloro-3-methylbutane  Reactant 2 = H2O  Product 1 = 3-methyl-2-butanol…

Q: Complete the following reaction

A: The diethyl carbonate is an ester. It is an ester of carbonic acid and ethanol. the molecular…

Q: CI CI + En Br HO

A: We have been given different starting materials and we have to synthesize the asked products. Since…

Q: 5. Complete the following reaction. (Mention the name of all reactants and products) + HNO, I.…

A: Since we only answer up to 3 sub-parts, we’ll answer the first 3. Please resubmit the question and…

Q: ? 1)Br2 2)H2O

A:

Q: d) C43- CH -C=c-H ) CiHy - C4-C=C-H Z HC! -> ラ=H>-コ- 1) 03 2) zn /H30+ f) CHエム Zn ( Cu) HBr 2 Li h)

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Q: OH a) HO. CI b) OH c) CI H d)

A: From given  For each reaction given its reaction type is mentioned along with explanation as follows

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.