Но-S-CI || 4 h, 20-25 °C Benzenesulfonyl chloride 77%

Q: CH3CO3H

A: In presence of per acid ,ketone molecule undergo Baeyer villiger rearrangement. Among two alkyl…

Q: Br Propose a mechanism for the reaction shown here, which takes place under conditions that favor an…

A: Given: To propose a mechanism for the given transformation which takes place under conditions that…

Q: most likely mechanism for the following reaction.

A:

Q: Consider the interesting cascade transformation below. Provide a detailed mechanism including all…

A:

Q: Please illustrate mechanism and product NH, HO Br

A: Alcohol is a weak acid and it reacts with a base to form alkoxide ion. The given compound contains…

Q: Draw a complete, detailed mechanism for the following 1. R'—ОН, Н reaction. R-C=N 2. H20, НО R OR'

A: The above reaction is an acid catalyzed reaction of nitrile with an alcohol which results in the…

Q: Provide a complete, detailed mechanism for the reaction CH;CH,OH shown here.

A: A complete and detailed mechanism for the given reaction can be provided as

Q: Me Oz C Me Oz C

A: Wittig reaction is the reaction of an aldehyde or ketone with the ylide generated from a phosphonium…

Q: How can do this reaction please O perpose mechanism

A: We have to carry out the following transformation. Also we have to give the mechanism of this…

Q: Rank the following substrates in order from slowest Sy1 reaction to the fastest. Br -Br Br A в D…

A: SN1 reaction is commonly known as unimolecular nucleophilic substitution reaction,  in this reaction…

Q: Draw the complete, detailed mechanism and the products for each of the following reactions.

A: Hello. Since the question contains multiple sub-parts, the first three sub parts are solved. In case…

Q: Consider the following reaction: AICh Toluene MECOCI Me- COME TICI How are these products being…

A: The complete step by step mechanism to formation of above product is give in attached image.

Q: Q2. Complete the following reaction. Show mechanism CI

A: “Since you have asked multiple question, we will solve the first question for you. If you want any…

Q: ive the complete mechanism for the reaction below. The major product should be that of something…

A:

Q: For each of the following reactions, draw a complete, detailed mechanism and predict the major…

A: . When aluene react with Bromine in water medium we got addition     product . Nucleophite attack…

Q: Draw a veasonable mechanism for this reaction that involves free radicals. CoH hv DH cat. OH Ph H,C

A:

Q: For each reaction, draw the complete mechanism and the major organic product(s), paying attention to…

A:

Q: Draw the complete, detailed mechanism for the following reaction.

A: Base abstracts a hydrogen atom from CH3NO2 and it generates a good nucleophile (-CH2NO2). This…

Q: e Tson t

A:

Q: PPH3 OC, H в + R H. PPH3 A CI

A:

Q: Consider the interesting cascade transformation below. Provide a detailed mechanism including all…

A:

Q: Br NaOEt ELOH

A:

Q: Ticls, k H2, Pdle CH3 Pooduch

A: In presence of TiCl3, McMurray coupling is occurred.  Followed by reduction of alkene .

Q: NH2 For the reaction shown here, draw the complete, detailed mechanism and major product. 1. CH3I…

A: The expected mechanism and products of the given reaction have been described below.

Q: Draw the complete, detailed mechanism for the reaction shown here and predict the major products,…

A:

Q: The reaction shown here proceeds via a carbocation rearrangement. Draw a complete, detailed…

A:

Q: Consider the following reaction scheme (note that the reagent shown above the arrow is DBN"). Draw…

A: DBN is a sterically hindered bicyclic non-nucleophilic nitrogen base.

Q: Mechanism. Provide the complete mechanism for the reaction below. You must include appropriate…

A: Interpretation- We have to provide the complete reaction mechanism for the given reaction as above…

Q: can you show the mechanism?

A: The solvent TsOH is known as tosylic acid. It is categorized as a solid that remains soluble in H2O,…

Q: Mechanism. Provide the complete mechanism for the reaction below. You must include appropriate…

A: Hydrolysis of Imine gives carbonyl group and amine.

Q: HBr, ROOR

A: Addition of HBr in presence of peroxide follows Anti-Markonikov's addition around alkene in which…

Q: Consider the following step during free radical substitution reaction. CH3 + CI• > → CH;CI What is…

A: Correct answer is Termination. It is the termination step of the reaction free radical substitution…

Q: Given the information below, write out a reasonable mechanism for the reaction. Where not provided,…

A: Since, change in concentration of KI does not have any effect on rate of reaction, so, it is SN1…

Q: PLEASE DRAW THE FULL MECHANISM FOR THE FOLLOWING BROMINATION REACTION FOR A THUMBS UP!! 'N Br3 -I…

A: Note : Pyridinium tribromide is source of bromine. N-acetyl aniline reacts with bromine produces…

Q: НО NaOH (CH3),N (CH3),NCH,CH,CI Can you show this mechanism please?

A: Nucleophilic substitution biomolecular reaction (SN2): The bimolecular nucleophilic substitution…

Q: Mechanism. Provide the complete mechanism for the reaction below. You must include appropriate…

A: Acid-catalyzed Transesterification reaction: is a reaction which converts an ester(reactant or…

Q: -Predct final Droduct Show Mechanis ms oftautomerization Hysoy

A: Hydration of alkyne with aqueous H2SO4 and HgSO4.

Q: Draw the complete mechanism for this reaction. p-CH3- CgH4– SO;H + H3C-OH

A: The organic conversion helps in the conversion of one organic compound into other compounds. This is…

Q: n-C,H,,CI- (CH,)CI NaCeC-H Na, NH, →B- KCN D- Of A E-H/N F

A:

Q: Draw a mechanism to account for the reaction shown here, which scrambles the isotopic labeling

A: The diene reaction with Alkynes is a Diels – Alder reaction.

Q: Carry out following conversion. Provide suitable reagents, reaction conditions and also mechanism…

A:

Q: (SYN) A student wants to carry out the reaction shown here. Explain the problem(s) associated with…

A:

Q: Br Ph-Li Br

A: Reaction of 1,1-dihalocyclopropane  with Ph-Li yields the majour product allene. Reaction: When…

Q: Br ОН Br

A: Given reaction;

Q: Draw a complete reaction mechanism that demonstrates why the product is obtained. Hig why the other…

A: The organic reactions proceed with a variety of reaction mechanisms. If a reaction is guided by one…

Q: H* HO OH

A: At first -C=O,take H+,than -OH attack to the carbonyl group. -OH is not good leaving group,so it…

Q: Provide the mechanism for the 1st reaction in this synthesis: OH .CI SOCI2 Mechanism NOT Required

A:

Q: Draw the structure of all products of the mechanism below. H-C=C -OH + H-Ö-CH, H. it

A: Due to presence of lone pair electrons in the O atom, alcohols like methanol can act as nucleophiles…

Q: 6. Explain why halogenation occurs twice in the following reaction. Ch₂ NaOH give both answer asap…

A:

Q: (a) HÇI (b) Br HBr

A: Alkenes reacts with the halogen acids and undergo addition reaction to produce alkyl halides via…

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.