Propose a plausible step by step mechanism for the following transformation H30*/heat `OH

Q: Complete the following reaction by adding major product. „Br + NAOCH3 CH,OH (solvent) hv • Br2 c)…

A: “Since you have posted a question with multiple sub-parts, we will solve first three subparts for…

Q: Propose a plausible mechanism for the following transformation. но to 1) H-CEC: Na 2) H20

A: When epoxide is treated with sodium acetylide (HCCNa) , then initially lone pair of oxigen of…

Q: Give a reasonable mechanism for each indicated reaction above. Use auditional sheets, make sure you…

A: On treating the given alkene with Hg(OAc)2, intermediates (I & II) and product (III) are formed.

Q: H;O H,SO, (cat)

A: This reaction involves formation of carbocation intermediate which exapnds ring to get stable…

Q: Propose a mechanism for the following reaction.

A: A mechanism for the following reaction has to be proposed

Q: Propose a reasonable mechanism for each product in the equations below. OH H2SO4 / H20 HO Br OH Br,…

A: First reaction is the epoxide ring opening in the presence of acidic condition and the hydroxide…

Q: b) Propose a detailed reaction mechanism for the following conversion. он Acetone HCI но но. -OH OH…

A: Acetone /HCl is used for the protection of syn-1,2-diol. For protection with acetone/HCl glucose…

Q: Propose a plausible mechanism for the following transformation: معلی معلم OH H₂O* OH

A: H3O+ is hydronium ion. It is used as a catalyst in this reaction.

Q: Provide a step by step mechanism for the following transformation. NH2 N2* HCI, NaNO2 H20

A:

Q: Propose a mechanism for the following reaction:

A:

Q: 14. Propose a mechanism for following transformation. M₂O 0

A: In this question, we will write the details mechanism steps by using curved arrows for the given…

Q: (CH3),COCH3 HI (CH3)½CI CH3I + + H20

A: In this question, we have to find out the correct answer of given problem by the help of the…

Q: Propose a mechanism for the following conversion ОН + H;0

A: We have given the organic reaction and we have to find the mechanism of the reaction.

Q: Propose a mechanism for the following reaction:

A: The given reaction is represented as follows:

Q: c) Write a detailed mechanism for the following transformation: OH CH;OH H,SO, (cat)

A:

Q: Which is the best method for the following transformation? OH A. 1. BH3, THF 2. H₂O₂, OH- B. H¹, H₂O…

A:

Q: Propose an elicient Synthesis Tor trne Tollowing transiO OH The transformation above can be…

A: At first propene undergo HBr addition in presence of peroxide (anti-Markownikoff's addition) to give…

Q: Propose a plausible mechanism for the following transformation. 1. OsO4 2. H3O*

A: Osmium tetra oxide is used to form vicinial diol on alkenes. After that pinacol-pinacolone type…

Q: Provide a plausible arrow pushing mechanism for the reaction below. OH LOME TSOH, H20 OMe

A:

Q: Propose a mechanism for the following reaction:

A: A Grignard reagent is an organomagnesium compound which can be described by the chemical formula…

Q: following

A:

Q: Propose a mechanism for each of the following reactions Br (a) CH3-CH2-C ECH + 2HB1 CH3-CH2-Ç- CH3…

A: Mm

Q: Propose mechanisms compatible with 1) and 2) of the following reactions.

A: Since we know that HBr adds with alkene by ionic mechanism in absence of peroxide so Markovnikov's…

Q: Suggest a) OH Br OH b) с) O-CH3 HO

A:

Q: Provide a plausible arrow pushing mechanism for the reaction below. 1 eq. H20 Но. MEOH OMe cat. H-A…

A:

Q: Propose an efficient synthesis for the following transformation. H. The transformation above can be…

A:

Q: Propose a plausible step by step mechanism for the following transformation. H30+, heat

A:

Q: Provide a plausible arrow pushing mechanism for the reaction below. You may abbreviate the…

A: This is an example of Diels-Alder reaction followed by cyclization and aromatization.

Q: The transformation above can be performed with some reagent or combination of the reagents listed…

A:

Q: Propose a plausible mechanism for the following transformation. HO 1) H-CEC: Na 2) H3Oʻ

A: The functional group is a key component that pertains to a molecule and it involves a characteristic…

Q: Provide a plausible arrow pushing mechanism for the reaction below. 1 eq. H20 + МеОн HO, OMe cat.…

A:

Q: Propose a mechanism for the following reaction:

A: The chloroform reagent taken is attacked by the electron rich double bond from the octadiene.

Q: Provide a plausible arrow pushing mechanism for the reaction below. OH OMe TSOH, H20 OMe

A: The answer is mechanism

Q: Propose a mechanism for the following reaction:

A: Please find below the reaction mechanism

Q: Propose a mechanism for each of the following reaction: CH3 H20 Br но CH3

A: In this reaction mechanism step first formation of carbocation step second in the ring opening and…

Q: NaOCH3 HOCH3

A:

Q: Br Br2 OH

A: In the given reaction, the first step of the reaction is the addition of the bromine to the double…

Q: Show the reagents for the conversion below: OMe

A:

Q: Propose a mechanism for the following reaction. -NH2 -NH-

A: To solve this problem we have to write the mechanism of the given reaction .

Q: Propose a detailed reaction mechanism for the following conversion. он НО Acetone HCI но. он OH HO

A: In this question, we have to find out the correct answer of given problem by the help of the…

Q: Propose a mechanism for the following reaction:

A:

Q: II] Propose a mechanism for each of the following reactions : Br 1) CH;OH OCH3

A:

Q: Choose the best reagent (A-E) for carrying out the following conversion from the list provided…

A: Given : structure of reactant and products.  Here oxidation of alcohol is happening.

Q: 1. Complete the multi-step synthesis below by filling in the missing reagents in boxes (a) through…

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

Q: Q4-) Obtain following diazo compound in two steps by writing mechanism and write necessary starting…

A: Given diazo compound formed by coupling reaction of diazonium salt.

Q: 30 Cl2 H20

A: Since the alkyne group is electron rich. Hence it will attack on Cl2 and form a intermediate with…

Q: Propose an efficient synthesis for the following transformation. The transformation above can be…

A:

Q: HCI CH3-CH2-CEN CH3-CH2-C-OH + NH,CI H2O

A:

Q: Provide a plausible arrow pushing mechanism for the reaction below. 1 eq. H20 MeOH Но. OMe cat. H-A…

A:

Sulfur Functional Groups

Many organic molecules contain sulfur functional groups and have their own importance in chemistry as well as biology. Some of the organic molecules which contain sulfur functional groups and the corresponding sulfur functionality is given below: