Predict the reaction of  methyl 3-oxocyclohex-1-ene-1-carboxylate with LiAlH4

Q: Predict the mononitration products of the following compounds.  m-cresol (m-methylphenol)

A:

Q: Predict the final product Y of the following reaction sequence. H3C, CH3 pyridine CH2 он он Pd(lI) •…

A: The formation of the Intermediate compound and X is shown below.

Q: Predict the products of the following reactions.(a) cyclohexylmethanol + TsCl/pyridine   (b) product…

A: These are organic reactions

Q: Predict the product(s) of the following reaction: OCH₂CH3 1. CH3CH₂MgBr 2. H30*

A: When ethylcyclohexanoate treated with Grignard reagent (ethyl magnesium bromide) and simultaneously…

Q: Predict the major products of dehydration catalyzed by sulfuric acid.  (a) pentan-3-ol       (b)…

A: a) The given compound is pentan-3-ol

Q: Predict the major products for the reaction of 1-methyl-1,2-epoxycyclopentane with H2SO4 in ethanol

A: The reaction of epoxide with acid and bases proceeds through the mechanisms of Sn1 and Sn2. The…

Q: For the following reaction, explain the likely mechanism including why it leads to the less…

A: From given reaction  Initially a mechanism is shown as each step followed by the explanation of why…

Q: Predict the product obtained when 1-pentyne reacts with two equivalents of HBr

A: When HX is added to terminal alkynes, addition occurs according to Markovnikov’s rule in which…

Q: (а) CH3 1. ВНз CH3CH2- CH3 2. NaOH, H2O2 H

A: Hydroboration oxidation transforms an alkenes into a alcohol .It carries out a net water addition by…

Q: Br CH2 1. PPH3 1. PPH3 Br H3C- 2. BuLi 2. Buli BuLi

A:

Q: Predict the product of the following addition of bromine to 1-methylcyclopentene in water. Br2 H20…

A:

Q: Predict the most likely mechanisms which occur when 2-iodo-2-methylhexane is heated in ethanol.

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Q: CH3CH,CH,CH,MgBr ,ether H;0*

A: In Grignard Reagent, the alkyl group is directly attached to magnesium metal and because of high…

Q: From the structure of the products expected to be obtained by dehydrohalogenation of 1.…

A: Haloalkanes undergo elimination reaction (dehydrohalogenation) on heating with KOH in presence of…

Q: 1. The 3,5-dinitrobenzoate esters of the epimers shown below both yield 3-cyclopenten-1-ol upon…

A: The reactivity of any molecule depends on its stability. The more any molecule is stable, the more…

Q: Predict the major products for the reaction of 1-methyl-1,2-epoxycyclopentane with(a) sodium…

A: Ring opening in basic condition:  Nucleophile attacks the less substituted carbon atom like SN2…

Q: Predict the most likely mechanisms which occur when 2-iodo-2-methylhexane is heated in ethanol. OS…

A: Here are required to find the mechanism for the reaction .

Q: Predict the product obtained when 1-pentyne reacts with H2SO4, H2O, HgSO4:

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Q: Dehalogenation of vicinal 3,4 Di-bromides Hexane by Zn and aceton its give Give Cyclo-Hexene I O…

A:

Q: 1. Predict the product and write the systematic reaction mechanism for the reaction of benzoic acid…

A: Carboxylic acids when treated with alcohols in presence of inorganic acid as catalyst results in the…

Q: Predict the product when cyclohexanone reacts with aqueous sodium hydroxide at 100°C. IV II II O 1)…

A: The structure of cyclohexanone is illustrated as follows: The structural formula of cyclohexanone…

Q: Predict the product of the following reaction. CH, + CHBR3 + (CH3),CO K+ -

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Q: O3 CO2 + HO-CCH,CH CH;CCH,CH(CHO)2 ?? Zn

A:

Q: Predict the major products you would obtain from the sulfonation of the followin compounds: a)…

A:

Q: 3. Propose a mechanism for the formation of the 4 alkenes shown below from the reaction of…

A: hydroxy group abstract hydrogen from sulphuric acid and OH will convert into good leaving group…

Q: + NH3 + `Br Br +°NH2 OMe Me OMe + N. Cl

A:

Q: Predict the product obtained when 1-pentyne reacts with H2, Pt:

A: Here, we have to find the product that will be obtained when 1-pentyne reacts withH2, Pt.

Q: Predict the major products of the following reactions.(a) 2,4@dinitrochlorobenzene + NaOCH3

A: Ipso attack: The entering nucleophile replace the substituent, which is already present in the…

Q: Predict the product from the following reaction. CHBR3 + (CH3)3CO K+ (Z)-3-Methyl-2-pentene

A: Given reaction,

Q: I. Cu2+ + OH Cl,C-C-H m. Ág(NH,), HO- + H,0 Cl,C-C-H

A:

Q: Predict the product obtained when 1-pentyne reacts with R2BH followed by H2O2, NAOH:

A: We will determine the end product by given question using the proper reagent as mentioned in the…

Q: CH-CH-CH-CH, + CH,-CHCH 13-Butadiene Acrolein The product of this reaction is cyclohexane-4-…

A: Given Reactant Given Product

Q: H2SO4, HNO3 Br2, AIC; `N' H2SO4, SO3 90°C

A:

Q: Predict the product for the following reaction. CH;OH/ H2SO4 OCH, ** OCH OCH3 OH OCH3

A:

Q: 4. Complete the outlined reaction sequence by drawing structures for the major products expected.…

A: A species with a larger size can easily accommodate negative charge. In other words, in a large size…

Q: What is the expected major product result from the acid- catalyzed hydration of…

A: We have given that  What is the expected major product result from the acid- catalyzed hydration of…

Q: Identify the starting material in the following reaction sequence.

A: Given reaction:

Q: Predict the product obtained when 1-pentyne reacts with NaNH2 in NH3 followed by MeI

A: 1-pentyne is a terminal alkyne and the reagent sodamide can deprotonate the terminal hydrogen.…

Q: Predict the major products of the following reactions.(a) 1,2-dichloro-4-nitrobenzene + NaNH2 (b)…

A: Given reactions, (a) 1,2-dichloro-4-nitrobenzene + NaNH2 (b) p-nitrotoluene + Zn + dilute HCl (c)…

Q: 1. Predict the product and write the systematic reaction mechanism for the reaction of benzoic acid…

A: Fischer esterification: In this reaction, when carboxylic acid reacts with an excess of alcohol in…

Q: What would you expect the product of the following reaction to be? он OH NAHGO, он он OH OH

A:

Q: Predict the reaction of methyl 3-oxocyclohexane-1-carboxylate with NaBH4/ h20 show the mechanism

A: Sodium borohydride (NaBH4) is a hydride donor, so act as a reducing agent. NaBH4 reduces aldehyde…

Q: 3. Propose a mechanism for the formation of the 4 alkenes shown below from the reaction of…

A:

Q: When the ketone below is treated with methylmagnesium bromide, two products are formed. Based on…

A: The reaction taking place is given as,

Q: Describe a sequence of reactions by which hept-1-yne can be straightforwardly prepared from…

A: The answer is given as follows

Q: Predict the product of the following chemical transformation: CH3 1. ВНз, THF 2. H202. ОН OCH3 CH3…

A: Answer

Q: Predict the mononitration products of the following compounds.  m-chlorotoluene

A: Given compound is, m-chlorotoluene

Q: Predict the products of the following reactions. 1-(bromomethyl)-2-methylcyclopentene, heated in…

A: The product of the following reaction has to be predicted. 1-(bromomethyl)-2-methylcyclopentene,…

Q: HCl 40 °C а.

A: In this question, firstly we will Identify the product and then draw the Reaction mechanism.  You…

Q: Propose an interpretation of the following result: the hydrolysis of allyl chloride (which involves…

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.