2.) 1.) iPrMgBr но 2.) H*/H2O

Q: 1. Give a synthetic route (hint: protecting group). OH

A:

Q: Use the appropriate reagent used in the reaction. (d),(e) please!!

A: Here we have to mention the appropriate reagent for reaction d and reaction e-

Q: Classify following solvent as protic or aprotic                 CH3NO2

A: Protic solvents are those which contain protons bonded with high electronegative atoms like oxygen…

Q: Draw the major product of this reaction. Ignore inorganic byproducts and CO2.

A: We have to give the major organic product of the given reaction. Here the ozonolysis of a…

Q: H2N- -ОН HO SOCI, Ме ОН Ме Ме

A: Given,

Q: Fill in the appropriate reagent or starting material in each of the attached reaction.

A: In this reaction , we can see that , there is a formation of thiol in the product side of the…

Q: Which of the compounds below has the greatest molar solubility? Each one’s Ksp is in parenthesis.…

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Q: Consider the following reaction. cat. ACOH el H2N-NH2 Toluene (reflux, remove H2O) a. Draw a…

A:

Q: List all the reagents necessary for this reaction: ???

A: Hydrogenation Reaction is the reaction of unsaturated compound with gaseous hydrogen to form…

Q: Indicate the reagent needed for the below reaction: н он

A:

Q: and CN are only source of C atoms OH

A: s Parts 4 & 5 of Gordon Reid's series showed, even the simplest analogue filters mess with your…

Q: What are the steps and reagents used?

A: Applying concept of organic synthesis and reagent.

Q: Draw the major product of this reaction. Ignore inorganic byproducts. Assume that the water side…

A: We have to predict the product of given reaction.

Q: Provide the synthetic route for the following reaction?  (CH3)2CHCH2Br ----> (CH3)2CHCH2CH2CH2NH2

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Q: [4] In STEPS 9-10, a hydroxide ion causes the anhydride to break down and cleave into two products.…

A:

Q: Make a solvent extraction scheme to separate the following compounds: он H3CO NH2 он a. b. с.

A: Liquid-liquid extraction is a well known extraction procedure to separate two or more compounds…

Q: Draw the arrow-push mechanism of the reaction! maior minor

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Q: Provide a plausible arrow pushing mechanism for the reaction below. CI 2 eq H20 +

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Q: Which statement is/are TRUE about acetylide anions? I. The alkylated product is poor with primary…

A: There are three statements about acetylide anoins :  1) The alkylated product is poor with primary…

Q: Rearrange this equation to isolate c. a = b ( - ) C =

A: Given equation is : a = b (1c-1d)  Rearrange the equation and determine the value of c = ?

Q: Classify following solvent as protic or aprotic                NH3

A: Aprotic Solvents are solvents that cannot display hydrogen-bonding. Protic Solvents are solvents…

Q: F;C. HCI ZI

A: IMPORTANT POINTS: In this type of question where precursor is asked ,here hypothetical hit and…

Q: What is the best reagent to use for this reaction? Lon La HO O HCI O HO*, H2O O SOCI,, pyridine

A:

Q: white reagents ب الله GH for each.

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Q: Ph Ph МСРВА Но HO.

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Q: ? OCH3

A: Carboxylic acid reacts with the two molecules of the Grignard reagent to form the tertiary alcohol.…

Q: please help me to make synthesis of chrysin (5,7-dihydroxyflavone) in 4 or more steps and start for…

A: Chrysin is a dihydroxyflavon in which the two hydroxy groups are located at positions 5 and 7. It…

Q: The product (name) in the reaction with H20/ acid catalyst and H9SO4. Pls draw the whole reaction…

A:

Q: Write the explicit formulas of A, B, C and D in the synthesis below.

A: A,B,C,D of this given synthesis need to be write . When cyclopentanone react with the Pyrrolidine it…

Q: In step 2 of the reaction sequence HCl is added to the basic reaction mixture after the reflux…

A: Virstatin is an isoquinonline alkaloid system. It is a drug used for treating cholera.

Q: Make a retrosynthetic analysis to design a synthesis plan. It should be ay least 2 steps synthesis

A:

Q: Br ОН - Br Но- + +

A: 1) Both reaction have same rate.  2) it is supported by polar aprotic solvents.

Q: NH base Z-

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Q: white reagents for each. - ∙Br OH шон

A: The first reaction is an example of halogenation of an alkyl halide whereas the second reaction is…

Q: Draw the major product of this reaction. Ignore inorganic byproducts. Assume that the water side…

A: The reaction given is,

Q: What are the reagents required to make the following conversions? ? ? a) b)

A: a) SN2 nucleophilic substitution reaction

Q: Draw all products, including stereoisomers, in attached reaction.

A: The nucleophilic substitution reaction involves the removal of a group bonded to a carbon center…

Q: Perform a retrosynthetic analysis (please include - disconnection etc) and suggest a synthesis of…

A: The retrosynthesis method is used to determine the starting material by the fragmentation of the…

Q: 3. Give another dye that is made using diazonium salt chemistry/coupling reaction. Draw the dye as…

A: Azo dye:- These dyes are characterized by the presence of azo groups. The azo  groups coupled with…

Q: Synthesize attached product from the given starting materials using an organocuprate coupling…

A: Product from the given starting materials using an organocuprate coupling reaction has to be given.

Q: What is the outcome of the reaction sequence shown in the box? 1. Base 2. Allylbromide H3CO 3. НСІ,…

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Q: ? a. HO. b. NH, N. d.

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Q: NH2 NH2 TCI AICI3 aniline

A:

Q: What is the use of acetylide formation??

A: Acetylide anion is an anion formed by the removing the proton from the end carbon of the terminal…

Q: using the starting materials given below. Any reagent needed can be used and you may need more than…

A: Applying concept of organic synthesis and reagent.

Q: Explain the Nitration ?

A: Nitration is the addition of nitrogen to the the compound.

Q: Investigate what an acid-base extraction consists of and what functional groups in substances can…

A: In Acid-Base Extraction, we can extract the acidic functional groups (like Carboxylic acid) and…

Q: Explain Tautomerization with example?

A: Tautomerization

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.