Predict the major organic product for the following reactions.

Q: Provide the structure of the major organic product in the following reaction. CN

A:

Q: Which one of the molecules shown below prefers to exist as its enol tautomer?

A:

Q: CO,Et

A: Answer

Q: CH₂ CH₂ CH3-CH₂-C- CH₂ CH3 h CH₂ CH3 The IUPAC name for this compound is

A: • Find the longest carbon chain that has the highest number of substituents. This chain is called…

Q: Which of the following is a weak nucleophile?

A: A nucleophile is an electron rich species that has atom with negative charge or lone pair. For…

Q: Draw the product for this organic chemistry question

A: We are given a reaction in which 1-pentyne react with NaNH2/NH3 followed by MeI, we have to draw the…

Q: Draw the organic product that results from the following reaction. Do not draw inorganic side…

A: Reaction of benzene with mixed acid (conc HNO3 + conc H2SO4) at 50-600C, produce nitrobenzene. A…

Q: Consider the reaction scheme shown below. HCI [1] HO. (a) Provide a detailed mechanism for reaction…

A: This reaction will occur via 3 step. In first step protonation then Water molecule eliminate to…

Q: Question 18 Which of these compounds would exist primarily in an enol form? d

A: Generally keto form is most stable than enol form, both exist in equilibrium.

Q: Provide the structure of the major organic product of the following reaction. ONa Br

A: Nucleophilic substitution is a reaction where an electron-rich nucleophile attacks an…

Q: Explain the below ? Carbanions are nucleophiles

A: Nucleophiles are electron rich species which donates electrons to electron deficient species. Eg.…

Q: 3) Provide the structure of the major organic product of the following reaction Br 8 NaNH,

A: Since, In the given reaction, NH2 act as nucleophile and it attacks the electrophilic centre and Br…

Q: Predict the product(s) for each of the following organic reactions. Draw the structure, but do not…

A: Given reactions are:

Q: From naphtalene and any other organic or inorganic compund you want, synthesize the following…

A: Synthesis of desired product involves multiple steps. These are : sulfonation (TCP), Bucherer…

Q: Providwe detailed solution and give the explanation of the concept...

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Q: Compound X gives mostly substitution when treated with sodium ethoxide. Which of the following is…

A: To find out the structure from the list of given molecules that after elimination reaction with…

Q: Provide the structure of the major organic product of the following reaction NaCN

A: Reaction of nucleophile and epoxide occurs through SN2 mechanism. Nucleophile attacks the carbon of…

Q: None

A: Step 1: Explanation: Beta-hydroxy aldehyde, or ketone, on treatment with acid undergoes dehydration…

Q: Propose a sequence of reactions to synthesize the target compound below from the indicated starting…

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Q: B) Provide the minimum reagents required for the following syntheses below. Me. Me. OMe HO,

A: In the given reaction 1, ester undergoes hydrolysis to produce carboxylic acid in the presence of…

Q: Synthesize the following compounds with any starting materials you'd like (within reason!)!

A: We have to  synthesize of 1-phenyl-1-butyne from suitable reactants and reagents.

Q: HgSO4, H₂O H2SO4 Q

A: Addition of water to alkyne takes place through Markovnikov rule. Addition of water to alkyne gives…

Q: Mechanism: Provide the mechanism for the following reactions. 1) NaOEt 2) Hао

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Q: OMe

A: The product has a cyclopropane ring in place of double bond of 1st substrate. The double bonded…

Q: Give the major organic product for the following reaction

A: We have to give the major organic product for the given reaction.

Q: Provide the curved-arrow mechanism to account for the following electrophilic aromatic substitution…

A: Chlorination of benzene: This reaction is an example of an aromatic electrophilic substitution…

Q: 1) Explain the formation of the MAJOR product for the reaction shown below. Your explanation should…

A: An arrow always depicts from a region of high electron density to low electron density ; that is…

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.