Mercuric oxidation in water, followed by NaBH4 reduction results in Markovnikov addition of water. Draw the mechanism and predict the major organic product. 1st attempt O See Hint NaBH4

Q: Curved arrows are used to illustrate the flow of electrons. Using the provided starting and product…

A: We have to draw the complete mechanism of the given reaction scheme. Introduction: E1 elimination…

Q: :C: H :CI: :CI: H. CH3 C=C H -CI: H3C-C-C-CH H3C CH3 CH3 Add curved arrows for the first step. Draw…

A: The curve arrow is given below

Q: from

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

Q: Consider the energy diagram shown below, which statement is Potential energy Reaction coordinate (A)…

A: Potential energy diagram is a diagram where the potential energy of the reactant and product is…

Q: Please drau the Fouooing in the most Stable chair Form.Ju8tih Strueture your chobre. HO

A: The substituents in the chair form of cyclohexane experience unfavourable 1,3-diaxial interactions…

Q: s sugar X a reducing or a non-reducing sugar?   Reducing, because one/both of the rings can open…

A: The carbohydrate containing free aldehyde or ketone groups in its molecular structure is said to be…

Q: Terminal alkyne is considered a more acidic compound because it has a lower s character. True or…

A: In this question, we will discuss about this Statement is true or false.  You can see details…

Q: 6.The three compounds below can form a carbocation under aqueous acidic conditions. Draw the…

A: When an alkene reacts with acid it gives carbocation intermediate

Q: 2. a) b) Ez Draw the products of each / elimination Росниня H #3 (111 |||| H3 C H Ф OCH₂CH3

A:

Q: cr Ald3

A: Applying concept of fredalcraft alkylation with consideration of steric effect.

Q: Which alkene has (E) configuration? а. b. c. d.

A: E–Z configuration is the method of describing the absolute stereochemistry of double bonds.

Q: :0:

A: Nucleophilic substitution reactions: these are the type of reactions in which nucleophile reacts…

Q: Rank the overall bond strain of the cyclic alcohol molecules enumerated below based on a decreasing…

A: We know that According to Baeyer's strain theory, the stability of cycloalkanes is dependent on the…

Q: 1. Explain why a carbonyl C=O bond is protonated at the lone pair while and alkene C=C bond is…

A: A molecular orbital diagram is a graphical representation used in chemistry to illustrate the…

Q: ip the chair and draw the other chair conformer. Circle the more stable conformer and brlefly…

A: Interpretation: We are provided with reactants and we have to give missing products.

Q: Noting the curved arrows, draw all the product(s), organic and inorganic, of the following reaction.…

A: This is a reaction between hydronium ion and a primary amine.

Q: For the reaction can someone please synthesize the given products from the given reactants. Multiple…

A: The explanation of the organic reaction is given below

Q: 17.) Sketch an energy diagram for a reaction that has... a. b. C. d. Low-energy reactants,…

A: An energy profile diagram, often referred to as an energy reaction diagram, is a visual…

Q: [Review Topica] [References) How many kinds of chemically non-equivalent hydrogens are there in each…

A: Chemically non-equivalent hydrogens are obtained when different hydrogens have different surrounding…

Q: Are indicated atoms nucleophilic, electrophilic or neither? Explain. CI

A: Three question based on electrophilic or nucleophilic nature of attacking species, which are to be…

Q: На, Pt

A: H2/Pt carriers out hydrogenation reaction with alkene and form alkane.It reduces the compound (…

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

A:

Q: Noting the curved arrows, draw all the product(s), organic and inorganic, of the following reaction.…

A:

Q: Name or draw as appropriate. IUPAC rules apply. OH H H H

A: Determine the IUPAC name of compounds. is a worldwide organization that assigns a specific name to…

Q: A B Energy Energy Br Br TM = Reaction Coordinate ||| CH3OH heat CH3OH heat Energy QUO C Energy…

A: In given reactions alkyl bromide is converted into alkene in the presence of methanol and heat.So,…

Q: Which of the following systems are conjugated?

A:

Q: Draw major product for each Rxn below

A: We have been given two organic reactions band we have been asked to draw major product for each…

Q: and/or Exo product Endo Product

A:

Q: H,C CH, heat H,C-O. + .0-CH,

A:

Q: E ر

A: Defined as the state corresponding to the highest potential energy along this reaction coordinate.

Q: Draw bith the higher molecular weight prlduct and the lowe weight product

A: This is a SN2  type reaction:

Q: {Ph)_CHC(CH:)_CC(CH,)_CH(Bn)CHO

A: The explanation is given below-

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: H H : 1D -H HN-H H H- H+ Reset Drawing

A: Interpretation: We have to write reaction between ammonia and HCl using bond arrow.

Q: НА, СНЗСH2ОH

A: Mechanism = To be determined

Q: Using arrows, show the electron rearrangement that takes place in the reaction.

A: The given reaction is a type of pericyclic reaction. Pericyclic reactions are those reactions which…

Q: Draw two major products of wedge and dash bonds to indicate stereochemistry where appropriate.…

A: It is reduction of alkene, syn-addition of hydrogen will occur.

Q: Schrock or Grubbs catalyst

A: This is an example of alkene metathesis

Q: Draw the alkene product. Select Draw Rings More / | c H 1. Ph3P 2. n-butyllithium 3. acetone

A:

Q: Give a clear handwritten answer of this reaction Draw the condensed of line angle structure formula…

A: Saytzeff's Rule: H+ will be eliminated from that ẞ-carbon from where the most substituted alkene is…

Q: H H3C-C + :CI: H,C - c - ČH3 CH, ..

A:

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.