C,H5- -C,H5 но- ETOH C,H5 C,H5

Q: SH S-S 2 + 2HI

A: For the conversion of thiol to disulphides in the lab, we use Iodine in the presence of base  and…

Q: Propose a mechanism and predict the major product. Cl2 hv

A: The reaction between alkanes and Cl2 in presence of light i.e hv is known as chlorination reaction.…

Q: Reagents required to carry out the following transformation are OH Select one: O A. joso, iNaHSO B.…

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

Q: 17. OH P+ + Hz t > CH3 CHCH, CH2 CHy

A: H2/Pt give reduction of aldehyde and ketone but not give the reduction of carboxylic acid . And this…

Q: 1. Propose a synthetic route for the desired products. a. b. &=&m OH OH HO CH3 OH

A:

Q: Which of the following is a major product of the reaction sequence shown (1) NaH/THF (A) (B) (2) HO,…

A:

Q: HO

A: In the given reaction the cyclohexanol is oxidized into cyclohexanol. The oxidation of the secondary…

Q: 85. a. Propose a mechanism for the following reaction: CH30 + Br Br

A: mechanism is follows as:

Q: Но -NH2 4. Use ANY needed reagents to effect the following transformation. draw the product draw the…

A: GIVEN:-

Q: e- Et,N OTS H. CH;CN/H,O 65% 1 2

A: For the reaction    The mechanism involves radical cyclization. Radical is formed by the electron…

Q: Propose a stepwise mechanism for the following reaction: CH2OH OCH2CH3 CH2OH OH CH2OH H H30* H. H H…

A: First profanation of Oxygen  Elimination of ethyl alcohol, formation carbonation and carbonation…

Q: Indicate how the following compounds can be synthesized from cyclohexanone and any other necessary…

A: a.

Q: Propose a mechanism for each of the following reactions:

A:

Q: Devise a synthesis of each product from the given starting material. More than one step is required.…

A: a.

Q: Consider the following reagents. A) H30* B) OH- C) CO2 D) Mg/THF E) KCN F) SOCI2 G) NABH4 H) LAH I)…

A: In the field of organic chemistry, Grignard reagents are particularly valuable organometallic…

Q: 8-6 Propose a mechanism for the following reaction. 0 CH3 CH3 H,C- CH3 HC PME, (2 equiv.) H,C "CH3…

A: There are different type of reaction in case of organometallic chemistry that are: (1) Oxidative…

Q: 11. Propose a mechanism for the following reaction: OH H₂SO4 Heat

A: When an alkene reacts with an acid, it leads to the formation of a carbocation.

Q: Indicate how the following compound can be synthesized from the given starting material and any…

A: LDA is a strong base. It is used to extract the ‘H’ from the less hindered side. It further…

Q: Draw a mechanism for the following reaction: но- O- CH, H,C- CH, H;C CH3 H,C CH, Он

A: The reaction of alcohol in the presence of sulphuric acid (H2SO4) produces more substitued alkene.…

Q: Identify the needed reagents in the following scheme: Br CH2OH HO OH сно b. C. а. d. е. f. -1

A: here cyclohexanone is undergoing certain chemical reaction using different reagents to form trans…

Q: Synthesize the following compounds using cyclohexanol, or any organic reagent that has 4 or fewer…

A: since you have posted question with multiple subparts, we are entitled to answer only first three…

Q: H,C 8 CH3 CH,O° H,C CH;OH CH3

A: An epoxide ring is a heterocyclic ring formed by two carbon and one oxygen. Due to angle strain, the…

Q: Which of the following is a major product of the reaction sequence shown? (1) HO HO (2) CH;CH,M…

A:

Q: What is the final product of the following sequence of reactions? 1) A diethyl ether 2) H30* PB13 Mg…

A:

Q: 3. A). Provide the necessary reagents to accomplish the following transformation. A) CH3 -NH-CH-CH,…

A:

Q: ite the structures of A-C and mechanisms of the following reactions. (i) Me2CuLi (i) PhMgBr N' HCI H…

A: In the above reaction, first step is formation of enamine Second step is reaction of Gilman Third…

Q: b) Predict a mechanism for the following reaction: Ph. Ph. H,N. Ph Ph H,N

A: Given reaction: We have to write the mechanism of the reaction.

Q: Propose a mechanism for the following reaction

A: Aldol reaction: It is a reaction in which carbonyl group reacts with enolate of aldehyde and ketone…

Q: Propose a mechanism for the reaction shown below. a) CI OH O NH2 + CI Heat NO2 NO2 b) NO2 HNO3 H2SO4

A:

Q: Propose a mechanism for each of the following reactions:

A: a) Please find below the reaction Since O is more electronegative than Cl, hence first attack is…

Q: 7. Propose a mechanism for the following transformation. H* `NH2

A: In the mechanism of the above reaction ; 1st step involves the protonation  2nd step : attack on…

Q: U18 18 HCI + H2O С. 18 `OH + H2O CH ОН CH

A: Acid catalyzed reaction with water :  In presence of acid , and water acetic acid can inter-convert…

Q: Draw a stepwise mechanism for the following reaction, which results in ring expansion of a…

A:

Q: OH H;O +

A:

Q: CH-CE CH CH2-C-CH3

A:

Q: H,0 Cat TSOH но OMe OMe MEOH cat. TSOH -H0

A: Ring opening reaction of epoxides goes through SN2 mechanism.

Q: Propose a mechanism for the following reaction:  2 C5H11OH C5H11-O-C5H11 + H2O (pentan-1-ol…

A: Ethers are formed from the alcohols. This reaction is acid catalysed and it involves the SN2 type…

Q: Reaction of benzylmagnesium chloride with formaldehyde yields alcohols N and P after protonation.…

A: The Benzyl magnesium chloride undergoes electrophillic addition reaction with formaldehyde to form…

Q: Q4. The major product(s) of the following E2 reaction is/are: CH CH,ONa Br CH3 E2

A: Biomolecular elimination (E2) reaction:E2 reaction involves a one-step mechanism in which…

Q: What product forms when the compound below is treated with Benedict's reagent? СНО H-C-OH CH,OH A)…

A: Benedict reagent is a mixture of sodium carbonate, som citrate and copper sulphate pentahydrate. It…

Q: OH CH3 CH3 H,SO4, `CH3 `CH3

A: Since there is lone pair electrons on double bonded O in the reactant. Hence it will take proton…

Q: A a. Draw the structure of both products B and C of these following transformations. ( 1) O3,…

A:

Q: Give the major product from A-E Give the major product trom A-E. the HBr D H2O2 H2 A Ni Ch H/H2O E C…

A: Different reagents are used for the synthesis of a compound (product) from the different compounds…

Q: Propose a mechanism for the following reaction. (Hint: The rate of the reaction is much slower if…

A: Given reaction:

Q: 3.4 Propose a stepwise mechanism for the following reaction: CH,OH OCH,CH3 CH2OH OH CH2OH H30 H H H…

A: Detail mechanistic pathway is given below

Q: Reaction of p-cresol with two equivalents of 2-methylprop-1-ene affords BHT, a preservative with…

A:

Q: Propose a mechanism for the following reaction:

A: The reactant undergoes E1 elimination reaction by forming a carbocation and then a 1,2 alkyl shift…

Q: What is the major product for the following sequence? A A X B В Your answer C D D 1. HBr 1.…

A: In step first there is overall elimination reaction and most substituted alkene formed. In step 2…

Q: 3. Choose the reagents necessary to complete the following transformation. H, + H H. А. КMnO,, Но B.…

A:

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.