9.16 Draw the products of each reaction. OH HCI HI HO HBr a. b. H С.

Q: Draw a stepwise mechanism for the following reaction.

A: The reactant undergoes reduction and ring opening to form the given product. The mechanism of this…

Q: Draw a stepwise mechanism for the following reaction.

A: This reaction involves 6 steps to form the final product and here, there is electron movement…

Q: Draw a stepwise mechanism for the attached reaction, which involvesboth a Diels–Alder reaction and a…

A: To Find: To draw the stepwise mechanism for the given a Diels-Alder and a nucleophilic acyl…

Q: H OTos С. d. a. b. H OTOS H OTOS

A:

Q: Draw a stepwise mechanism for the following reaction.

A:

Q: Draw the product formed from ring-closing metathesis of each compound .

A: (a) In the given metathesis reaction, ethene is obtained as a by-product and the ring closure occurs…

Q: Draw a stepwise mechanism for the following reaction.

A:

Q: Draw a stepwise mechanism for the following reaction.

A:

Q: Draw a stepwise mechanism for the following reaction. он Cro3 H2SO4, H2O

A: The chromic oxide, CrO3 gets converted into chromic acid, H2CrO4

Q: Draw a stepwise mechanism for the following reaction: HO H,SO,

A: protonation of alcoholic group loss of leaving group carbocation rearrangement  deprotonation…

Q: 6. Draw the products formed from nitration of each compound OH OH b. а. CH3 ČHa

A:

Q: Draw a stepwise mechanism for the following reduction.

A: Since LiAlH4 is strong reducing agent. (It produces H- for reducing the molecule). Hence it will…

Q: Draw the products formed from nitration of each compound.

A: (a) Nitration product of p-cresol is, OH group is powerful ortho para directing group than Me so…

Q: Draw a stepwise mechanism for the attached reaction

A:

Q: Draw a stepwise mechanism for the following reaction.

A: To form the target molecule, the conversion of pyranose into furanose takes place. The mechanism of…

Q: Draw a stepwise mechanism for the attached reaction.

A: Mechanism for the given reaction is given in step 2

Q: 2. Which reaction will proceed faster A or B? CI H2S H2S 'CI A B

A: If i draw these molecules in chair conformations and lock t-butyl groups at equitorial position for…

Q: What products are obtained from the reaction of the attached compound with one equivalent of Br2,…

A: Interpretation - To determine which product formation take place when one equivalent of Br2, using…

Q: Draw the product of each reaction.

A:

Q: Draw a stepwise mechanism for the following reaction.

A: Since NaH is a strong base Hence it will remove the D from the reactant and form a -ve charge And…

Q: 6. Draw the products formed from nitration of each compound он он a. CH3

A:

Q: Draw a stepwise mechanism for the following reaction.

A: The molecular fragment getting depart from its original molecule with a heterolytic cleavage is…

Q: Draw a stepwise mechanism for the following reaction.

A: 1.protonation of an alcoholic group in the presence of acid HBr Removal of water for the formation…

Q: A B

A: This is an elimination reaction.  Here HCl is removed or eliminated to get an alkene.

Q: Draw a stepwise mechanism for the following reaction.

A: A stepwise mechanism for the given reaction can be drawn as

Q: Draw a stepwise mechanism for the attached reaction

A: The mechanism for the given reaction involves the formation of a secondary carbocation which…

Q: Draw a stepwise mechanism for the following reaction. RO Lewis acid or HA ∞0 HO A RO

A:

Q: β-D-Glucose, a hemiacetal, can be converted to a mixture of acetals on treatment with CH3OH in the…

A: A stepwise mechanism for this reaction has to be drawn. The reason two acetals are formed from a…

Q: 6. Draw the prod uc ts formed from nitration of each compound OH он b. CH3

A: Two aromatic structures whose nitrated product is to be reported.

Q: Draw a stepwise mechanism for the following reaction.

A: Since LiAlH4 produces H- ions in the solution And since H- ions is a strong nucleophile Hence it…

Q: Draw a stepwise mechanism for the following reaction.

A: A stepwise mechanism for the given reaction can be shown below,

Q: Draw a stepwise mechanism for the following reaction.

A: The given reaction is acid catalyzed dehydration of 20 alcohol with sulfuric acid (H2SO4). In step…

Q: What products are obtained from the reaction of the attached compound with one equivalent of Br2,…

A: The reaction with Br2, using FeBr2 as a catalyst causes the electrophilic aromatic substitution…

Q: Draw a stepwise mechanism for the following reaction: HBr HO Br

A:

Q: Draw a stepwise mechanism for the following reaction.

A:

Q: Draw a stepwise mechanism for the following reaction, which involves both a Diels–Alder reaction and…

A: [4+2]-cycloaddition of a conjugated diene and a dienophile (an alkene or alkyne), an electrocyclic…

Q: Draw a stepwise mechanism for the following reaction.

A: To draw the stepwise mechanism of the below reaction

Q: Draw a stepwise mechanism for the following reaction.

A: Since the carbon making C=O is having partial +ve charge due to attached with electronegative O and…

Q: Draw a stepwise mechanism for the following reaction.

A: The reagent which is being used is CF3COOH is highly acidic in nature and in the reactant, a base is…

Q: Draw a stepwise mechanism for the following reaction: H,SO, Part 1:

A:

Q: Draw a stepwise mechanism for the following reaction.

A: LiAlH4 ( Lithium Aluminum Hydride) is a powerful reducing agent. This can be used for reducing…

Q: Draw the product formed in each attached reaction.

A: Since we only answer up to 3 sub-parts, we’ll answer the first 3 sub-parts. Please resubmit the…

Q: Draw the product of each reaction. [1] NaCN Br [2] LIAIH4 [3] H2O а. [1] DIBAL-H b. CEN [2] H2O

A: We have to predict the product of each of the reaction.

Q: Draw a stepwise mechanism for the following reaction.

A: In the first step, the pyranose form of D-Glucose is converted into a stable linear form of…

Q: Draw a stepwise mechanism for the following reaction.

A: In presence of H2SO4, alcohol undergoes dehydration reaction. For the given compound, the mechanism…

Q: 9.78 Draw a stepwise mechanism for the following reaction. OH NAOH

A:

Q: Draw a stepwise mechanism for the following reaction.

A: Here the reactant present is 1,3-cyclohexadiene. The reaction undergoes in the presence of DCl ((2H)…

Q: (a) Draw a stepwise mechanism for the conversion of A to B. (b) What product would be formed if C…

A: LDA is used as s strong base which abstracts H+ from the more acidic position. This generates an…

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.