CH3 CH3 OEt NH3 A в D least reactive most reactive

Q: In electrophilic aromatic substitution reaction by drawing the structures of the compounds given…

A: Electrophilic aromatic substitution :- Electrophilic aromatic substitution simply means attack of…

Q: Correct Answer List Question List (4 images) (Drag and drop into the appropriate area) Most reactive…

A: The compounds given are,

Q: OH

A: IMPORTANT POINTS:   BENZENE is converted to benzaldehyde by gatterman koch synthesis, in this…

Q: o electrophilic aromatic substitution

A: Electrophilic substitution reaction may be defined as the reaction in which electrophile is…

Q: Identify the electrophile and the nucleophile in each of the following reaction steps and then draw…

A: nucleophile are the one which has excess electrons or electron rich to donate to a electrophile. And…

Q: When we have discussed the enol-keto tautomerization of ketones in class, the isomerization has been…

A: During the keto-enol tautomerism, it is observed that the molecule prefers to stay in keto form when…

Q: The two reactions that follow involve nucleophilic substitution at an acyl carbon. For each…

A: The Question is based on the concepts of chemical reactions. we need to explain the mechanism for…

Q: Aromatic compounds which contain non-carbon atoms (e.g., O, N, S) as part of the cyclic conjugated a…

A: 1.) there is only 1 lone pair on oxygen atom (because 1 lone pair gets involved in resonance so…

Q: Explain why the hydroxyl group present in phenol increases the rate of electrophilic aromatic…

A: Organic reactions are those in which organic reactant react to form organic products. In the given…

Q: ? Br

A: 1. For conversion of benzene to benzoic acid Reagent = CH3 , Anhydrous AlCl3 Followed by alkaline…

Q: Rank group of compounds from most reactive to least reactive toward electrophilic aromatic…

A: When the benzene ring has electron-donating groups, then the benzene ring has more reactive to…

Q: Arrange the compounds in  set in order of decreasing reactivity (fastest to slowest) toward…

A:

Q: nucleophilic

A: Dear student I have given answer to your question in the image format.

Q: Rank imidazole, pyrrole, and benzene from most reactive to least reactive toward electrophilic…

A: Electrophilic substitution reaction- The replacement one atom or group of atom from reactant species…

Q: When attempting to synthesize an alkyne, why is the hydrogen on the right abstracted instead of the…

A: This can be explained as:

Q: Define central relationship between nucleophilicity and basicity in comparing two nucleophiles?

A: Nucleophilicity follows basicity across a row means that, as basicity increases from right to left…

Q: In base-catalyzed halogenation of acetone, the second (and third) on the same carbon. How do you…

A: Acetone(ketone) is carbonyl compoumd Carbonyl group attached to 2 methyl groups  Hydrogen's which on…

Q: Rank the reactivity of the following alkenes toward acid-catalyzed hydration from most reactive to…

A: Hydration of alkene in the presence of acid proceeds with the formation of a carbocation…

Q: Arrange these compounds in order of reactivity towards electrophilic aromatic

A: The reactivity of aromatic compounds in electrophilic substitution reaction is depends on groups…

Q: Arrange the compounds in  set in order of decreasing reactivity (fastest to slowest) toward…

A: Electrophilic substitution is the substitution of H of an aromatic ring by an electrophile. The…

Q: Substitutions on aromatic rings are generally carried out by electrophilic substitution, but for the…

A: A question based on aromatic compounds that is to be accomplished.

Q: TO b) A A CI B B NH3 CC13 C OMe most reactive most reactive least reactive least reactive

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Q: Rank group of compounds from most reactive to least reactive toward electrophilic aromatic…

A: An aromatic compound is more reactive toward electrophilic substitution reaction when it contains an…

Q: Arrange the compounds in  set in order of decreasing reactivity (fastest to slowest) toward…

A: Given compounds,

Q: HBr (excess) Br Br

A: Firstly, the addition of H+ takes place across the triple bond which gives rise to two carbonations,…

Q: Given aromatic compounds with the following functional groups attached to them what is the order of…

A: Given functional groups,    NO2, COOH, and benzene    Benzene, ester, ketone    CH3,  CH2Cl , CHCl2…

Q: A bicyclic heterocycle aromatic ring with one N atom and the rings are of different size.   a…

A: A bicyclic heterocycle aromatic ring with one N atom and the rings are of different size

Q: Name and Draw the structures of all possible chemical (Electrophilic aromatic substitution)…

A: Halogenation of phenol is a Electrophilic aromatic substitution reaction. Hydroxyl group of phenol…

Q: The nitro groups on the benzene ring in the reactant serve two purposes. One is to let you know what…

A: Nitro group shows -M as well as -I effect. Therefore, it is electron withdrawing group and it…

Q: 2. Which of the following compounds would be considered anti-aromatic?

A: Step 1:Hückel's rule for aromaticity, antiaromatic and non aromatic compound are :-…

Q: electrophilic aromatic displacement reaction by drawing the structures of the compounds given below…

A: Aromatic Electrophilic substitution reactions:

Reactions of Ethers

Ethers (R-O-R’) are compounds formed by replacing hydrogen atoms of an alcohol (R-OH compound) or a phenol (C6H5OH) by an aryl/ acyl group (functional group after removing single hydrogen from an aromatic ring). In this section, reaction, preparation and behavior of ethers are discussed in the context of organic chemistry.

Epoxides

Epoxides are a special class of cyclic ethers which are an important functional group in organic chemistry and generate reactive centers due to their unusual high reactivity. Due to their high reactivity, epoxides are considered to be toxic and mutagenic.

Williamson Ether Synthesis

An organic reaction in which an organohalide and a deprotonated alcohol forms ether is known as Williamson ether synthesis. Alexander Williamson developed the Williamson ether synthesis in 1850. The formation of ether in this synthesis is an SN2 reaction.