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

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: 3. Propose a plausible mechanism for the following transformation НО. YOH H2SO4

A: Applying concept of formation of electrophile and electrophilic substitution on benzene ring.

Q: (b) Suggest a plausible mechanism for the following transformations R EGN (1) →? (2) MezSiCl (3)…

A: NEt3 is base. It will absrtact proton from methylene group and will form enolate.Since Si is a hard…

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: Provide a mechanism for the following transformation: OH Cro3 но. H30*

A: The mechanism of the given reaction is given below,

Q: a. Propose a plausible mechanism for the following Heck reaction TBSO Pd(PPH3)4 K2CO3 H. OTBS 2.

A:

Q: Propose a detailed mechanism for the following reaction: HO OH H₂SO4 O y

A:

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: F

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: Propose a practical "racemic" synthetic route for the following molecule. Me- HO. HO-

A: The synthetic root of the following molecule is as follows:

Q: B3. Write a detailed mechanism for the following Knorr Synthesis 1) (BUO-NO (0.5 equiv) , HCI A…

A: Preparation of pyrrole compound by using beta amino keto-ester and beta-keto ester is called Knorr…

Q: Propose a mechanism for the following reaction:

A: The given reaction is represented as follows:

Q: 5. Propose a plausible mechanism for the following transformation:

A: Given that : We have to propose a mechanism for the following transformation :

Q: Propose a mechanism for the following reaction H2SO4 CH3-0-H OCH3

A:

Q: 4. Provide a arrow pushing mechanism for the following transformation. H3O+ Br2

A:

Q: II] Propose a mechanism for each of the following reactions : NaOCH3 Br 2)

A: Here i have explained the mechanism of this reaction

Q: 5. Propose a plausible arrow pushing mechanism for the following transformation. он H+

A:

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

A:

Q: Propose a detailed, step-wise mechanism for the following transformation, make sure to SHOW all…

A: Desulfonation reaction In organic chemistry, the desulfonation reaction is the hydrolysis of…

Q: Minor product via E1 for 2-butanol and HCl?

A: Alcohol reacts with hydrogen chloride to give substitution and elimination reactions, depending on…

Q: Write a detailed mechanism for this transformation. OH HCI НО НО H2O -OH

A:

Q: CH3 CH3 CH3 H3C-Ċ-CI CH3 ČH3 + HC1 AICI3

A:

Q: HO NH2 H3O+ HO NH HO Но

A: 4-(2-aminoethyl)bnzene-1,2 diol reacts with acetaldehyde in the presence of acid, it results in the…

Q: 3) write a detailed mechanism for the following reaction: Br hv light + HBr + Br2

A:

Q: 5. Provide a mechanism for the following transformation: H2SO4 ÓH

A: We have to predict the mechanism for given reaction.

Q: 2. Propose a stepwise mechanism for the following transformation, producing the observed…

A: Grignard reagent, RMgX is a useful reagent in organic synthesis. Where X be any halogen. Epoxides…

Q: 2. Draw a detailed mechanism for the following reaction and give the structure of the product. NH2…

A:

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: Propose a detailed mechanism for the reaction below. لعلام , AICI3

A:

Q: 1. Provide a detailed, stepwise mechanism for the reaction below: (CH3)2CHCH2CH2CH21 + CN-…

A:

Q: froblem of The Day1 Suggest an eficient synthesis for the following Transformation and provide a…

A: The addition reaction of alkene takes place when it is treated with Br2. The mechanism of the…

Q: OEt 1. NaOEt 2. H3O*

A: The given reaction is,

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: iv) NGÔM, HO Heat

A: Note : Retro aldol followed by intramolecular aldol condensation. (For mechanism, see below).

Q: 1. Show a detailed mechanism for the following reaction and give the structure of the major product.…

A:

Q: 2) you Isobutane

A:

Q: Write a detailed mechanism for the following reaction. он Он H,SO4, H2O ÓH но

A: All steps mention in hand written solution.

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: 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: Select from the Table provided the reagent you would use to carry out each of the transformations…

A:

Q: Q6. Provide a step-wise synthesis for the following compound using benzene as a starting material.…

A:

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

A: To get more stabilized carbocation ring expansion takes place and the elimination will give the…

Q: II. Propose a suitable synthetic route to carry out the following transformations.

A:

Q: Stork developed the tollowing enamine reaction as an alternative to the Robinson annulation. Below…

A:

Q: Provide a plausible curved-arrow mechanism for the following transformation. سلاح 1) NaOEt, EtOH 2)…

A: This reaction mechanism follows the reverse process of Claisen ester condensation.

Q: 1. Show a detailed mechanism for the following reaction and give the structure of the major product.…

A: The detailed mechanism of the reaction is provided below in attach image.

Q: The product below can be prepared from cyclohexanone through the following reaction sequence? A) [1]…

A:

Q: но NH2 но NH Но Но

A: There are many mechanisms in organic chemistry such as nucleophilic substitution, nucleophilic…

Aromatic Compounds

Aromatic organic compound or aromatic system is an important class of hydrocarbons under the branch of organic chemistry. Aromatic compounds are also called arenas. The definition of aromatic organic compounds can be stated as a class of organic compounds with a planar cyclic ring of atoms bonded through alternated single and double bonds. Due to these alternating bonds, a peculiar feature termed as ‘resonance’, that is, delocalization of pi electrons or the electrons is shared within the atoms of the ring which are present in the aromatic compounds. The word ‘aromatic’ includes a Greek word ‘aroma’ which means smell, indicating that they were named as such due to the sweet odor they produce. Many well-known flavors such as vanilla, cinnamon, and few scents from flowers are extracted from aromatic compounds. Benzene with chemical formula C6H6 is a very common aromatic compound that contains six atoms of carbon held in the cyclic ring of alternate double bonds. It is also to be noted that not all aromatic compounds contain benzene ring. This can be explained by Huckel’s rule.