OH HNO2 NH2 H2N `NH2 OH 4,5-diaminopyrimidines 4-hydroxypyrazolo(3,4-d)pyrimidine aka: Allopurinol

Q: The major product of the following reaction is он H,SO, heat

A: First lone pair of OH will attack on H of H2SO4. See the written solution.

Q: H

A: The given problem is the conversion of aldehyde to a ketone compound basically. There are many…

Q: I = = = = + NH₂ Σ B Ph with the mechanism. H+

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

A: Detail solution is given below

Q: Predict the products for the following reactions by showing complete reaction mechanisms. Also,…

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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: ✓ Propose a plausible reaction scheme (show all reagents and intermediate product for each step) for…

A: We have to propose a plausible reaction scheme for the given reactions. The required reaction scheme…

Q: 2. Draw a reaction mechanism to explain the following reaction. OH (aq) LOH i. OH

A: We have to show the mechanism for the above given reaction in which a compound having epoxide ring…

Q: H * CH,NH2

A: This conversion is a multistep synthesis reaction.

Q: Provide missing reagents of the following reactions: Please explain

A: REACTION SCHEMES ATTACHED BELOWExplanation:

Q: HBr ROOR

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Q: Consider the following reaction: AICh Toluene MECOCI Me- COME TICI How are these products being…

A: The complete step by step mechanism to formation of above product is give in attached image.

Q: (b) OAc HOAC MsO

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Q: er. Br N- OEt N- OE

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Q: What is(are) the major final product(s) formed during the following sequence of reactions? OI Oll ON…

A: Ozonolysis: Alkene on reaction with ozone form carbonyl compounds.Wittig reaction: Carbonyl compound…

Q: Propose an efficient synthesis process for this transformation. HO,

A: Williamson Ether Synthesis: Williamson ether synthesis is a type of coupling reaction for the…

Q: Rxn F NaOH

A: The unimolecular nucleophilic substitution reaction (SN1) proceeds in two steps. In the first step,…

Q: Which is the major organic product of the reaction provided? A) Br B) Bra, hv Br racemic Br ** D)

A: In presence of light or heat halogenation of alkanes proceeds through formation of free radicals.…

Q: Complete the following reactions by providing the proper substitution AND the proper elimination…

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Q: KMnO4 H*/H₂O (A) COOH (B) -COOH (C) COOH -COOH (D) -COOH

A: KMnO4 is strong oxidizing agent in the presence of acid and this reagent oxidized to all benzylic…

Q: What is the major product of the following reaction sequence? H*, CH;OH

A: Epoxides are cyclic ethers with three membered ring containing oxygen atom. These can open up in…

Q: OMe cm Clz mCP BA MeO `OH

A: Given reaction is example of Baeyer-Villiger oxidation. The Baeyer–Villiger oxidation is an organic…

Q: 3. Draw the systematic reaction mechanism for between the reaction of isoamyl alcohol and acetic aci…

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Q: Mechanism. Provide the complete mechanism for the reaction below. You must include appropriate…

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Q: Complete the organic mechanism

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Q: Multistep Syntheses: Draw all the reagents as well as the major product of each stép necessary to…

A: Detail synthetic pathway is given below

Q: Br HO. +

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Q: Provide the structure of the organic products(s), which result in the reaction below. (Hint: it's a…

A: In nucleophilic substition reaction a nucleophile displace another group to form a product. If…

Q: In your own words, please describe the following reaction mechanism in detail, and also describe any…

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Q: (e) ⠀⠀

A: Diels-Alder reaction between cyclopentadiene and methyl vinyl ketone and subsequent ozonolysis of…

Q: Q5. Draw the all products and a detailed mechanism for the following reaction? -OCH2CH3 Br CH;CH2OH

A: When any Alkyl halide treated with sodium alkoxide, in Presence of ethanol , elimination Reaction…

Q: ~NBU2 HO NaOH H. CI ELOH

A: The first step of the reaction involves the acid-base reaction. The NaOH being a strong base will…

Q: OMe O OMe PdCl₂ (cat) A CUCI, O₂ H₂O

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Q: Meo Meo Meo, ...H Provide the reagents that would result in the given product.

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Q: f 2 но H +

A: -> Carbonyl compound reacts with alcohol in presence of acidic medium and form Acetal.

Q: Complete the following reaction with mechanism and a major product:

A: The first step is abstraction of most acidic proton by reaction with base (K2CO3) to form a…

Q: The reaction below is a base-catalyzed aldol reaction. O || CH₂-C-H CH3-C-H Ethanal (Acetaldehyde) H…

A: The aldol reaction is an organic reaction in which two carbonyl compounds reacts in presence of…

Q: E. 0 OH C-CO- -C n

A: The question is based on the concept of organic synthesis.We need to synthesize the product using…

Q: Add any remaining curved arrow(s) to complete step 4 of the mechanism. Modify the given drawing of…

A: In an organic reaction mechanism, a curved arrow represents the transfer of electrons. In an organic…

Q: Provide the product(s) and draw a step-by-step mechanism for the reaction shown below. Make sure to…

A: Step 1: Step 2: Step 3: Step 4:

Q: I need a detailed reaction mechanism of this synthesis

A: Dear Student Find the complete Mechanism

Q: Given the following reactants and reagents: OH ОН H₂SO4 (1) predict the product and (2) upload a…

A: An elimination reaction is a type of chemical reaction where a molecule loses specific atoms or…

Q: ... 1) NaOEt, EtOH, heat 2а) ВНз-THF 2b) H2O2, NaOH .. A + en OH + en OH ... + en но

A: 1)- E2 elimination occure. 2). Hydroboration reaction (syn addition).

Q: COCH3 NaBH4 / H₂O 1. excess LIAIH4 2. H₂O Br Mg/ether 1. 2. H₂O H

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Q: Mechanism. Provide the complete mechanism for the reaction below. You must include appropriate…

A: Given reaction is an example of Aldol condensation reaction, for the formation of above product two…

Q: HONH, CI- , NaOH

A: This is an example of condensation reaction in which hydroxylamine condensed with 1,3-dikketone to…

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.