2. Write the reagents and steps needed to perform the following synthesis (multiple steps may be needed).

Q: مشهد

A: Given is organic synthesis reaction.In given reaction epoxide is converted into ketone and alpha…

Q: Propose a synthesis for the following compound start with any reagents with four carbons or fewer.

A:

Q: Synthesise the target molecules drawn below using precursor chemicals within the following…

A: Synthetic organic chemistry involves the production of the target molecules by the combination of…

Q: Propose a multi-step synthesis to achieve the following transformation. Make sure to include all…

A: Given is organic synthesis reaction.In which reactants are alkene and benzyl bromide .The product is…

Q: 2. Show how you would carry out the following transformation as shown. More than one step is…

A: Given is organic synthesis reaction. The given reaction is,

Q: OCH3

A:

Q: Show how to bring about the following transformation.

A: A question based on ether synthesis. An aralkyl halide is prescribed for which the corresponding…

Q: Choose the correct order of reagents to complete synthesis. To preview image click here Step 1 Step…

A: The question is based on the concept of organic synthesis.We need to synthesize the product using…

Q: Propose a suitable synthetic route to carry out the following transformations

A: The above reaction is the conversion of carbonyl group into -CH2 which can be done by reduction.

Q: Propose a route to 1-butyl-4-nitrobenzene, using benzene as your only aromatic starting material.

A:

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: Show all steps in the synthesis of 4-methylaniline from toluene. Clearly show all reagents,…

A:

Q: Show how to convert the given starting material into the desired product. Note that some syntheses…

A: Cyclohexane on reaction with chlorine in the presence of sunlight or U.V.light gives…

Q: a) Propose a synthesis route to prepare the following product from the given starting material. Note…

A:

Q: 4. Propose an efficient synthetic route (along with intermediates) for the following transformation.…

A: Cyclohexane is a common starting material in various organic reactions due to its stability and…

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.