Following is a synthesis for albuterol (Proventil), currently one of the most widely used inhalation bronchodilators. CH,0 CH, Но CHO Но- -CHO -СНО NaOH CH,S-CH, DMSO, NaH Но- 4-Hydroxybenzaldehyde A B NH NH Но OH OH Но C D Albuterol

Q: Draw the major product(s) of the following reaction. H₂C=CHCH₂CH₂CH₂CH=CH₂ + 2HCl

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Q: ********* e) LiBH(S-Bu)3 (L-selectride) 65% ***** 1000

A: The reaction involves the reduction of ketone stereoselectively. The reagent L-selectride is an…

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A: Step 1:Step 2:The reaction simply follows the SN2 mechanism which is a most favoured solvent that is…

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Q: 2. Show the B-cleavage mechanism and product for following reaction -R R'

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A: Given compound,

Q: Which of the following is least likely to form a Grignard reagent? A B CHỊCH Ph3CCI Et3CCI…

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Q: dont provide handwriting solution ...

A: Step 1: -Cl group is converted to -CN. It is a nucleophilic substitution reaction.  -MeO group does…

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Q: Click the "draw structure" button to launch the drawing utility. What cyclic product is formed when…

A: In presence of base , diketone compound undergo intermolecular condensation reaction i.e. aldol…

Q: There is a missing reagent, provide a structure for it.

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Q: b) Draw the structure of the major product of perbenzoic acid oxidation (Baeyer-Villiger oxidation)…

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Q: ® which of the fillowing Erplain. aromatic, antiaromahe or nonaromMai are a) (9 f)

A: Condition for aromaticity are: 1. The molecule should be cyclic and planar. 2. The molecule should…

Q: Illutrate with equation the preparation of alkanes by: a. Wurtz synthesis b. Grignard synthesis

A: Alkanes are saturated hydrocarbons.General formula of alkane is CnH2n+2 Here we have to illustrate…

Q: a. Draw the structure of the tetrahedral intermediate INITIALLY-FORMED in the reaction shown. You…

A: (a)The structure of the tetrahedral intermediate

Q: ① Draw the Pdt. & Mechanism. H-I (Excess)

A: Step 1:  Step 2:Ethers are organic compounds characterized by having two alkyl groups attached to…

Q: d) e) type type a) LDA, THF b) BnBr, THF

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Q: Which of the following method is the best method for the synthesis of propanoic acid      A.)…

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Q: Be sure to answer all parts. Draw a stepwise mechanism for the following reaction: Part 1 out of 3…

A: We have to draw the stepwise mechanism of the given reaction.

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A: Organometallic compounds are defined as compounds containing a covalent bond between a carbon atom…

Q: 2. Draw the reaction scheme in ChemDraw depicting Strecker aldehyde starting from α-dicarbonyl.…

A: The aldehyde which is generated by the Strecker degradation reaction is called Strecker aldehyde.

Q: What is Lucas reagent made of? explain.

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Q: 4. Br MeO Meo Me 5. Me Meo

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Q: Show how you would synthesize this reaction.

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Q: Draw all alkenes formed from alkyl halide, and predict the major product

A: Zaitsev rule:According to this rule the more substituted alkene is formed as a major product.

Q: IZ ACOH A of 1) Mel 2) KOH Provide detailed mechanism of the above reaction using curved arrows.…

A: To provide detailed mechanism of the above reaction using curved arrows.

Q: 3) Draw the product formed when allylic alcohol (shown below) is treated with each reagent. A) H₂ +…

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Q: What is the product of this reaction sequence? В. OH OH 1. НО 2. LIAIH 3. H2O, H, heat С. D. OH, H*…

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Q: A reaction of a particular B-dicarbonyl compound that gives substituted or disubstituted acetic…

A: Introduction A β-dicarbonyl compound is a molecule that contains two carbonyl groups (C=O) separated…

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A: The reaction rate is affected by the nature of the alkene, with more nucleophilic double bonds…

Q: Reaction No. Reaction COOH Be H* CH;OH Heat 1) LIAIH4 2) H3O Ce

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A: Nucleophile  substitution  depends upon the leaving group .

Q: (a) Draw two different halo ketones that can form A by an intramolecularalkylation reaction. (b) How…

A: (a)

Q: 2C.) Provide missing reagent(s) in the box. Br OH

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Q: Synthesis of Glyciene by strecker method.

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Q: 10. Draw a complete curved arrow mechanism for the following reaction sequence. CC13H + KOt-Bu +

A: CCl2 carbene formation take place Carbene insert into alkene below the plane Explanation:

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.