When a reaction is desired between two incompatible reagents, what is useful to employ? A Protecting Group A Catalyst A Blocking Group Additional Heat

Q: Draw the structure of the major organic product for the following reaction:

A: Carbonyl compounds react with a secondary amine to form an enamine. Enamines are nitrogen analogous…

Q: Label the nucleophile and electrophile. For the electrophiles mark the place for nucleophilic…

A: Nucleophiles are the chemical species which have a pair of electrons to donate. They donate the…

Q: Do not give handwriting solution.

A: Chromic acid is used for over-oxidation of primary alcohol into carboxylic acid.. Its formula is…

Q: Consider the reaction conditions provided in the question(s) below question. Determine the type of…

A: Alkyl halide gives an elimination reaction by reacting with a strong base. E2 reaction involves a…

Q: NaH) (H Jo) Enolate anion (or H) Ketone or aldehyde

A: This reaction is an acid base reaction in which hydride ion from sodium hydride being a very strong…

Q: Please fill in the missing pieces [starting material, product(s), reagent(s), or no reaction] for…

A: For 1-bromo-2-methylcylopentene is reacted with NaOH since the alkyl halide is a vinyl halide.…

Q: the reactants and products. Name the final ester product. *draw your structures so the functional…

A:

Q: performing (the dehydration of cyclohexanol) is reversible and actually slightly endothermic. How…

A: Here we have to shift the equilibrium to product side of the reaction i.e dehydration of…

Q: How many electrons are involved in each of the following reactions? Part A) 2Al2O3→4Al+3O2…

A: A) 2Al2O3 --> 4Al + 3O2 The oxidation state of Al and O atom in Al2O3 are +3 and -2 respectively.…

Q: Consider the following:   Why is the oxygen atom selectively protonated? A) Oxygen is less…

A: Protonation means the attachment of a proton by a nucleophile it happens only when an nucleophile…

Q: what is the major product of the following reaction

A: Elimination reaction is takes place. So, Alkene is major  product.

Q: Draw structural formulas for the major organic product  reaction

A: Oxidation of primary alcohol to an aldehyde: The oxidation of a primary alcohol to an aldehyde can…

Q: What is the name of the reactant and the structure (only structure) of the product? o H₂O, H₂SO4

A: The objective of the question is to find the name of the reactant molecule and the structure of the…

Q: Why is it important that we are very careful in how much acid is added to neutralize the reaction?…

A: If too much acid is added during crystallization after neutralization value then acid will increase…

Q: What reactants would be needed to proceed the reaction?

A: A question based on reactions of alcohol. For the given conversion the reactants required need to be…

Q: When aniline undergoes addition to an electrophile, the carbocation intermediate has a variety of…

A: In the electrophilic aromatic substitution of benzene derivatives, the substitution of incoming…

Q: A substance which can be used with sulfuric acid to oxidize ethyl alcohol is O LIAIH4 O K2Cr207 O…

A: The structure of ethyl alcohol is as shown below.

Q: QUESTION 4: H₂C OH p CH3 CH3 H₂C CH3 CH3

A: An elimination reaction is a type of chemical reaction where several atoms either in pairs or groups…

Q: Indicate the product of the reaction ОН, H2O heat

A:

Q: What products are formed when each of the following reacts with HO−?  BF3+HO−⇌ CH3++HO−⇌…

A: Here BF3 , CH3+ , FeBr3 & AuCl3  reacts with OH-  to form adduct or stable molecules.

Q: theoretical yield for reaction theoretical mass for stilbene, acetic acid, and pyridinium tribomide…

A: From the reaction it is clear that one mole of stilbene reacts with one mole of Br2 in presence of…

Q: Select the phenols. There may be more than one answer.

A: We need to find the phenols and complete second reaction.

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.