draw the product

Q: Drawing an Enol and a Ketone Formed by Hydration of an Alkyne Draw the enol intermediate and the…

A: Enol intermediate and the ketone product formed in the reaction:

Q: -OH/H20 ACCI, pyridine H* /H2O

A:

Q: (a-b) (c-d) H₂O any languag CuCl -NEN + -NEN CuBr -OH

A:

Q: OH CH3

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

Q: What reagents ( A–D) are needed to carry out each reaction in the following sequence?

A: The reagent is added to the chemical reaction to see whether the reaction occurs or what product is…

Q: + `OH HO

A:

Q: a) from benzene Br b) from

A: Given reaction,

Q: Synthesize the products by drawing out reagents and intermediates along the way.

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

Q: Choose the best reagents to complete the following reaction.

A: Step 1: Step 2: Step 3: Step 4:

Q: Devise a synthesis for each compound, starting with methylenecyclohexane and any other reagents you…

A:

Q: (v) 2 + 2 Na Br

A:

Q: (i-j) NO2 (k)

A: In the first reaction, the amide is reduced into amine which is converted into quarternary ammonium…

Q: ОН

A: We have to draw synthesis of the following given compounds from the starting chemical as follows in…

Q: Show how to convert the given starting material into the desired product. Note that some syntheses…

A: Cyclohexane on reaction with chlorine in the presence of sunlight or U.V.light gives…

Q: HO 1. 2. OH Ph Ph of Ph 1. 2. Br. Ph OH Ph QIQ 1. 2. OH 1. Ph 2. OH Ph Ph

A: The question is based on the concepts of Organic reactions. we need to identify the reagent for the…

Q: но 3 но но Tamoxifen

A: Reagents and reaction conditions for each step

Q: Draw the MAJOR product for each transformation.

A: Enolate ion are produced form the carbonyl compounds having alpha hydrogens which are abstract by…

Q: The following reaction takes place in multiple steps, with a vital intermediate isolated after the…

A: Please find the answer in the attachment below. Feel free to raise any queries is there are any.…

Q: CH3 Br NO₂ COOH

A: The reactant is toluene and product required is 4-bromo,3-nitro benzoic acid.  Initial step is to…

Q: Propose a synthesis of the target molecule from the starting material(s) provided. Please be certain…

A: The conversion involves a series of reactions.The first step is the oxidation of the given steroid…

Q: Identify reagents by letter from the reagents table for each step in the following scheme. Some…

A:

Q: For the following reaction scheme, match the correct reagent to each reaction (A, B, C, D and E).

A: Here a sequence of reaction is given and reaction contains side chain oxidation, halogenation,…

Q: СН3 ? H3 G- - N-CH3 СН3

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Q: veactant CF3 Product НО CF3 Cl Teactant product 2) CH3 H,N. CH3 reactant CH3 preduct

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Q: Complete synthesis, show reagents and intermediate compounds.

A: The given amide can be obtained from the acid-amine coupling of diethylamine and…

Q: H₂C CH₂ NH3 slightly acidic (pH 4-5) 1)LIAIH in diethyl ether 2) H₂O

A:

Q: Br 1. Mg, ether 2. Со2 (a) 3. Н.О, Н OH H+ (b) HO, (с) NaHCO3 HO. ? HO. CI (d) K*OH (e) HO, 1. NaCN…

A: We have to provide the product or reagent for the following given transformations as follows in step…

Q: Show reagents and steps

A: Applying concept of organic synthesis and reagent.

Q: CH3-Br Ag,0 C5H13N N(CH3)3 H20 (heat) (еxcess)

A: Interpretation - To write the reactant in the following reaction sequence which is given as above in…

Q: Br ОН

A:

Q: 10. 다음 반응을 완성하기 위한 촉매/시약(a-i)을 쓰시오. HC H3C CH Br H CH3 CH;CHCH3 H H. (h) CH,CCH,CH, (i) (а) (g) HC…

A: Different reagents and catalysts are responsible for the different type of conversions from one…

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.