Propose a forward synthesis for one of the two molecules below, using benzene as your starting material. HO SO3H NO2

Q: Which best describes the major organic product of the following reaction. expoxide diol markovnikov…

A:

Q: Provide the major product of the reaction below. кино/ Heat COOM COOM COCH COCH COOM D

A:

Q: * aq. H₂SO4 OH

A:

Q: Phenols have lower pKa values than other alcohols due to the resonance stabilization of the…

A: More the pka value of an acid lower is its acidity.

Q: Rank the following compounds in order of increasing reactivity in electrophilic aromatic…

A: If benzene ring participates in electrophilic aromatic substitution reaction, then the ring must be…

Q: How can the following molecule be synthesized by reductive amination (with NaBH4)? Note that there…

A: Carbonyl compounds react with primary amine to form imine which can be reduced by NaBH4 to form…

Q: 1) [H*), HỌ 2) NaNH, 3) Etl 4) H3O+ 1) [H*]. HỌ 2) Etl 4) H30* 1) [H*]. HỌ 2) NaNH, 3) Etl 1) [H*].…

A:

Q: N. cat. H2SO HN H20

A: Given, The structure of products are; and In the reaction, carbocation goes into conjugation.

Q: Indicate the major organic product that would be formed under the conditions below: 1. ВН3 THF 2.…

A:

Q: Rank the following nitrogen-containing aromatic molecules in order of increasing basicity. least…

A:

Q: Provide a Ø synthesis for the following transformation N₂

A:

Q: H3C CH3

A: Using butanol i.e alcohol contains 4 carbon atom treated with kmno4 or cro3 this are oxidizing…

Q: What would be found in an HNMR of this compound? N- ·S O

A: Number of signals = Number of sets of protons in different electronic environment

Q: Provide a reasonable route to synthesize the following product from the given phenol. Show all…

A: The given reactant is a m-bromo phenol and the product is m-alkyl substituted phenol. So, we can…

Q: CH3 NO2 NH2 CH3 NH2 N' NH2

A: A base is  defined as a molecule that has the ability to donate an electron pair .

Q: Which of the following ranks the compounds in order of increasing acidity, putting the least acidic…

A: Acidic nature: Tendency to release proton In a row the acidity increases with the increasing…

Q: OMe OMe NO₂ NO₂ HCI 40 °C A A A

A: For the first reaction diene reacts with HCl at 40°C this leads to the 1,4-addition of conjugated…

Q: Provide an arrow pushing mechanism for the following reaction. Include protons and each step clearly…

A:

Q: Propose a synthesis of the following molecule from the given starting material. You may use any…

A:

Q: Provide a complete synthesis for the transformation shown below: OH (2) CH CI OH

A: For the given transformation, the steps required sequentially are photolytic  halogenation ,E2…

Q: . Please provide a forward synthesis for the following aromatic compounds using benzene as the…

A: Synthesis of given organic compounds is as follows

Q: Identify the functional groups in each constitutional isomer of C,H,NO. Select all that apply Isomer…

A: Question 1: The functional group is amine.An amine is a compound with a nitrogen atom attached to a…

Q: rank these compounds in order of increasing basicity 3 Rank these compounds in order of increasing…

A:

Q: Show how the enamine below can be synthesized. Then draw the resonance structure(s) for the enamine.

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

Q: Draw the major organic product of the Bronsted acid-base reaction between the compounds shown below.…

A:

Q: Rank the following four molecules according to the decreasing basicity of their NH2 group (1 for the…

A: This problem is based on general organic chemistry. Here we have to find out the basicity of the…

Q: Provide an arrow pushing mechanism for the following reaction. Include protons and each step clearly…

A:

Q: EtO₂C NO₂ NH₂OAc glacial HOAC benzene/A

A: Here ammonia being basic removes the acidic proton of active methylene group .

Q: 3. Draw compounds A-G in the space below the scheme using line notation ΟΞ A: hexanoic acid B:…

A:

Q: CH3 H,SO, HO

A: This reaction is known as internal electrophilic aromatic substitution reaction where benzene ring…

Q: NH₂ х CI НО. див ОН SH (1 eq) ОН pyridine ОН P205

A: Detail mechanistic pathway is given below to find out the product

Q: Propose a set of reactions to convert the starting material to the given product. NO2 OMe

A: The given transformation can be carried out in different ways.  But, I will show the most effective…

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.