raw a stepwise mechanism for the following reaction: Br CH3CH2OH

Q: Choose the correct product for the given reaction. HO LIAIH4 ? H20 HO. LOH HO H20 HO D. С. B. A.

A: LiAlH4 is astrong reducing agent, it can reduces carboxylic acid to alcohol

Q: 30.51 Draw the products of each reaction. a. b. O OCH₂ (CH₂)₂CO-OC(CH₂) Buli (initiator) BF₂ + H₂O

A: Note- Dear student , since the given question is a mutipart questions,so l solved first three…

Q: Draw the products of each reaction using the two-part strategy from Sample Problem 10.7.

A: EXPLANATION: The reaction of alkene with Hydrogen halide takes place by Markonikov addition.When an…

Q: Draw a stepwise mechanism for the following reaction. [1) NaOEt EtO OEt [2] [3] H,O, A

A: 21.59

Q: 52. Draw a stepwise mechanism for the following reaction. EIO i OEt 1) NaOEt 2) 3) H₂0* OEt

A: Concept based on the organic chemical reactions mechanism.

Q: Draw the product formed when each starting material is treated with LDA in THF solution at −78 °C.

A:

Q: Draw a stepwise mechanism for the following reaction and explain the stereochemistry of the product.

A: The protonation step is shown below.

Q: Devise a synthesis of each compound from cyclohexene as the startingmaterial. More than one step is…

A: Enantiomers are pairs of molecules having same connectivity with opposite three dimensional shapes,…

Q: h) Draw a stepwise mechanism for the following reaction. OH NH,OH MEOH

A: The stepwise mechanism of reaction provided below in attach image.

Q: h) Draw a stepwise mechanism for the following reaction. OH N° NH,OH MEOH

A: The reaction in which intramolecular transfer of proton is known as tautomerism.

Q: Draw a stepwise mechanism for the following reaction.

A: A stepwise mechanism for the following reaction is given below :

Q: When the following reaction is performed two products are obtained. a. Draw both of the products…

A: Bromination of ethyl benzene go through a free radical mechanism and it gives two isomeric…

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: Devise a synthesis of each compound from cyclohexene as the startingmaterial. More than one step is…

A:

Q: Draw the expected product of the conversion under photochemical conditions. Draw Rings Select hv…

A:

Q: Draw a stepwise mechanism for the following reaction.

A: LiAlH4 is lithium aluminum hydride acts as a strong reducing agent  In LiAlH4 hydrogen behave as…

Q: Draw a stepwise mechanism for the following reaction.

A: Given reaction,

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

A:

Q: Draw the product formed from a Michael reaction with the given starting materials using −OEt, EtOH.

A: SOLUTION: Step 1: The Michael reaction or Michael addition is the nucleophilic addition of 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: 35 conversion. Identify suitable reagent (s) for the following N'ENCI H,C HC A Cu(l)C/dilHCI B…

A: The suitable reagent of the given transformation is

Q: Draw the major organic product for the reaction. H₂O cat. TfOH -H Select Draw с Rings H O More

A:

Q: Draw the stepwise mechanism for the following reaction. 1. LDA, THF 2. Br

A: The given reaction is  To find: Mechanism for the given reaction

Q: Identify the correct product of the reaction shown below. A a В b C D d H2SO4 (cat.) OH + но OH OH…

A:

Q: Lx Grve Up? In each reaction box, place the best reagent and conditions from the list. 1) 2) 3) 4)…

A: In this question, we determine all best Reagent for this transformation. I will give complete…

Q: 1. Name the starting compound and then draw a reaction. stepwise mechanism for the following Cl2 .Cl…

A: In this question, we have to draw a stepwise mechanism for the following reaction.

Q: An allylic alcohol contains an OH group on a carbon atom adjacent to aC—C double bond. Treatment of…

A: Since the reaction of an alcohol with HCl can go through both SN1 and SN2 reactions. Hence when it…

Q: 19. Draw the most likely product for the reaction. LOH acid catalyst heat a) b) HBr

A: We have to form the products of given reaction.

Q: An allylic alcohol contains an OH group on a carbon atom adjacent to a C − C double bond. Treatment…

A: Since the reaction of alcohol with HCl can go through both SN1 and SN2 reactions. Hence when it…

Q: Draw a stepwise mechanism for the conversion of dihalide A andcyclohexane-1,4-diol to polyether B in…

A: The stepwise mechanism is given below -

Q: Dimethyl cyclopropanes can be prepared by the reaction of an α,β-unsaturated carbonyl compound X…

A:

Q: One acetal can be converted to a different acetal by reaction with a diolin the presence of acid, a…

A: Given,

Q: Dimethyl cyclopropanes can be prepared by the reaction of an α, β-unsaturated carbonyl compound X…

A:

Q: When A is treated with aqueous −OH, the major product is compound B, which undergoes ester…

A: To find: The stepwise mechanism for the conversion of A to B

Q: Draw a stepwise mechanism for the following reaction.

A:

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 conversion of hex-5-en-1-ol to the cyclic ether A.

A: The mechanism of conversion is as given below:

Q: Draw a stepwise mechanism for the following reduction.

A: The mechanism of the given reaction involves ten steps. The first step is nucleophilic attack of H-…

Q: Q#6 Draw a stepwise mechanism for the following reactions. a) (b) HO. H2SO4 hex-5-en-1-ol

A:

Q: RUESTION 35 (1) SOCIZ What is the structure of the final Isolated product for the reaction to the…

A: When propanoic acid reacted with thionyl chloride followed by the addition of 2 moles of…

Q: Ме Ме. 'N' Me H O:

A: Concept- In the reaction there will be first addition of I2, and then elimination of HI.

Q: Draw a stepwise mechanism for the following reaction

A:

Q: A re the following reactions regioselective? 7) (3R)-3-bromo-3,4-d'methy Ihexane is refluxed with…

A:

Q: What is the major product formed in the following reaction? A A В C C D D E E H,SO. (conc.) он heat…

A: Alcohol in presence of concentrate acid undergo elimination reaction.  Water is eleminated as…

Q: Draw the product formed when each starting material is treated with LDA in THF solution at −78 °C.

A: The product formed when the given starting material is treated with LDA in THF solution at -78°C has…

Q: For the following reaction: a. Draw the missing starting material b. Show the complete stepwise…

A: This is an example of epoxide opening under basic condition. This is SN2 type reaction that…

Q: Quèstion 15 10. The major product that would form from the presented reaction scheme is? CH3 H2/Pd…

A:

Q: An allylic alcohol contains an OH group on a carbon atom adjacent to a C − C double bond. Treatment…

A: The two products shown in the above molecule is formed by the reaction when the carbocation is…

Diol

In chemistry there are so many chemical compounds that have a hydroxyl group but a chemical compound having two hydroxyl groups (-OH) is termed as a diol. It also implies the presence of two alcohols whereas polyols contain two or more than two hydroxyl groups (-OH). Glycol or 1,2-diol is an aliphatic diol that has two alcohol groups on adjacent carbon atoms. In industries, the most commonly used diol is ethylene glycol.