the major product of the

Q: 1) LAH 2) H0 OH heat ONa 1) NaOH 2) H,O" 1) Ph,P 2) NaH 3)

A:

Q: from

A: The steps for the given synthesis are 1. Chlorination of toluene  2. Formation of sulphide  3.…

Q: Draw the major organic product for the reaction. H Hg(OAc)2, H₂O acetic acid Incorrect Y.

A:

Q: draw the major product of this reaction O NaOCH₂CH₁, CH₂CH₂OH a

A: Organic reactions are those in which organic reactant react to form organic products. In the given…

Q: LiAlH4 and NaBH are used to? None are correct reduce arenes. All are correct reduce carbonyl groups.…

A: Lithium aluminium hydride (LiAlH4) and sodium borohydride (NaBH4) both are reducing agent.

Q: Explain why CH3CONH, is a stronger acid and a weaker base than CH,CH2NH2.

A: The reason for CH3CONH2 is a stronger acid and a weaker base than CH3CH2NH2 has to be given.

Q: CH3CH₂CH₂CHFCH₂CO₂H CH3CHBrCH₂CH₂CH₂CO₂ CH3CH₂CH₂CBr₂CH₂CO₂H

A:

Q: What reagent(s) would you use to convert the compound in part a to the product shown below? H…

A: Reactant -Product - The given reactant is an alcohol and the product to be formed is an aldehyde.…

Q: QUESTION 3: QUESTION 4: H OH OH NaBH4 LIAIH4

A: A classic example of reduction is rusting: it is when oxygen reacts with iron to form rust. In this…

Q: whats the  final products

A: This reaction is proceed by SN2 reaction mechanism. In which nucleofile attack from back side of…

Q: Which of the following would yield a positive Molisch Test? Oe. Methane Ob. O Cheerios Cholesterol…

A: Molisch test is an important test to detect the presence of carbohydrates in a given sample. In this…

Q: e. f. g.

A: Since you have posted questions with multiple sub-parts, we are entitled to answer the first 3 only.…

Q: I kefore unsaturated alpha beta) I

A: Here in the following given compound  we have  to indicate alpha and beta carbon atoms and to give…

Q: How to conert dicarboxylic acid to mono carboxylic acid explination with examples

A: Converting a dicarboxylic acid to a monocarboxylic acid typically involves decarboxylation, where…

Q: HO me PhCH₂OH, p-TSA toluene, reflux

A: An arrow always depicts from a region of high electron density to low electron density ; that is…

Q: Give the IUPAC name for the following compound: OH Give the IUPAC name for the following compound OH

A: Given :-    ------------------------------------------------------

Q: 1.) LIAIH, NH 2.) H,O* a.) b.) c.) но. NH NH Racemic d.) e.) но HO,

A:

Q: Which below has the most oxidized carbon? O Alkene O Alkane O Primary alcohol O Secondary alcohol A…

A: The compound which has most oxidised carbon among the given functional group is secondary alcohol.

Q: CI Zn/HC1

A: Given reaction,

Q: Curved arrows are used to illustrate the flow of electrons. Follow the curved arrows and draw the…

A: The addition of bromine to an alkene in a nonpolar solvent produces vicinal dibromo alkane.

Q: ...|| 1. Hg[OAc)>, Н,0 2. NaBH.

A: Please find your solution below : The given reaction is an example of oxymercuration-demercuration…

Q: Is this reaction, Oxidation, Reduction, or Neither? Problem viewing the image. Click Preview Here…

A: Organic reactions are those in which organic reactant react to form organic products.

Q: Rank the following in order of increasing basicity. coo coo" coo

A: Rank the following structures according to basicity

Q: What are the reactants needed to accomplish the synthesis? Products Products Starting materials…

A:

Q: 3. Draw an Energy Diagram and include the starting materials, intermediates, transition state, and…

A: An energy diagram of a chemical reaction displays the graphical representation of energies of…

Q: what happens when two ortho para directors are para from each other?

A: Electron donating group are the groups that add density into a conjugated system with the effects…

Q: O a. O b. C. d.

A: A 1,3-diaxial interaction occurs when two bulky substituents are in axial positions on the same side…

Q: The basic propety of concerete or cement motar is?

A: (i) It has a high compressive strength. (ii) It is free from corrosion and there is no appreciable…

Q: to llow ung reaction Assume you have enough of each reagont/ vea cton bo

A: The details solution for this is provided below in attach image.

Q: Which labeled carbon is the anomeric carbon?   Select one: a. A b. C c. D d. B e. F f.

A: Labeled A is anomeric carbon

Q: Major product (A) of the given reaction is CH, CI NaNH, →(A) liq. NH,

A: Given,

Q: 6. To draw the structures of final product and A Br 1. LDA 1. BuLi A 2. Mel 2. Br

A: Step 1: Step 2: Step 3: Step 4:

Q: Consider the molecule in the box. Which molecules (A-D) is/are diastereomers of the molecule in the…

A:

Q: Br NaOEt ELOH ....|||

A: In NaOEt/EtOH medium, E2 reaction occurs. For E2 reaction the stereoelectronic requirements is that…

Q: Give detailed Solution with explanation needed....

A: To determine the only product of the given reaction, we need to analyze the reaction of the provided…

Q: gar b) d) D Draw the product of the following reactions. D heat heat heat Lo heat

A:

Q: 1) 03 2) (CH3)2S 1) mCPBA 2) 1M HCI, EtOH

A: Nucleophile opens the epoxide ring from more substituted side in acidic medium.

Q: alkyne aromatic alkene alkyne aromatic alkene alkane alkane CH, CH,СССH, CH; (CH, ),CH, aromatic…

A:

Q: What is an appropriate name for the follow

A: Using rules of IUPAC nomenclature we can give name of given compound.

Q: Classify the following reaction as an oxidation, reduction, or neither with respect to the indicated…

A: Correct answer is neither oxidation nor reduction. Oxidation state of indicated carbon atom is not…

Q: What intermedlate is formed in this reaction? Click on a letter A through D to answer. НА H. А. H.…

A:

Q: OMe

A: The product has a cyclopropane ring in place of double bond of 1st substrate. The double bonded…

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.