Haloalkanes acts as an electrophilic centre . Explain

Q: Complete the following reaction sequence, giving structural details of all significant intermediates…

A: 1  -OH group is protect by the DHP Dihydropyrane

Q: NH2

A: The question is based on the concept of organic mechanism. this is an example of nucleophilic acyl…

Q: NH2 H* -H,0

A: Ketone when react with primary amine forms imine as a product.

Q: 4 pts Provide the structure of the major organic product. in the following reaction sequence. 1.…

A: Answer:- This question is answered by using the simple concept of chemical reaction of ketone with…

Q: During sulphonation of benzene, H2SO4 generates the electrophile SO2 O "HSO4 O SO3 O +H O

A: In this question, we will Identify which electronphile is generated from sulphonation reaction on…

Q: a. Complete the following reactions and outline the mechanism for the formation of the product: CH3…

A: Alcohols when treated with Halogen acid then formation of Alkyl Halide takes place.  The reaction…

Q: 5. Complete the outlined reaction sequence by drawing structures for the major product expected. Yo.…

A: Nitro benzene is meta directing towards electrophilic reaction.

Q: Using curved arrows to indicate electron movements, illustrate the steps involved in a polar…

A: The carbon atom which consists the positive charge and three bonds is known as carbocation.

Q: Provide a plausible arrow pushing mechanism for the reaction below. O-OtBu s-OtBu AHN. CO,Me 1. LDA…

A:

Q: Draw structures for A, B, and C in the following reaction sequence and identify the process that…

A: Solution-

Q: Describe stereoselective, regioselective, or chemoselective, the reactions below.

A: In case one we write the most stable structure in chair form, now their is two possibility to attack…

Q: ihe diagram below shows two synthetic pathways by which the compound W might be prepared. C3H;OH…

A: Stepwise reaction upto W from first path   Here first we chose oxidising agents and then followed by…

Q: d) BF3 OEtz 13 CH2CI2 ОTBS 78%, 19:1 d.r. 5 OTBS 7 8

A: 1. Here the recent given is a Lewis acid.  2. The Lewis acid is a species which is able to accept…

Q: toluene n-butanol reflux Dean-Stark trap 2 hours но но 4a 5. 1a

A:

Q: 2) Draw the arrow-push mechanism of the reaction: Br AICI3 action:

A: Lewis acid have vacant orbitals in which they can accommodate the lone pair of electrons. Example of…

Q: Br CH3 HC=C_H,C NH; líq. NaNH2 B A NH3, líq. Br 1. О `OH 2. Н,О, H* 2. КОН D +

A: Detail mechanistic pathway is given below

Q: Write the product of the reaction below and show the mechanism by which it is formed. но catalytic…

A:

Q: For each of the following reactions, predict the major product. 1. SOCI2 2. H2N (еxcess) HO, mCPBA…

A: 1) Reaction of carboxylic acid with SOCl2 produces acid chloride. Reaction of acid chloride with…

Q: H2SO4 H20

A:

Q: The initial reactive intermediate in the elimination reaction of 2-bromo-3-methyl-pentane is a…

A: Elimination reaction :-        Elimination reaction are mainly two type i.e E1 (Unimolecular…

Q: б. a) Write the reaction mechanism between 2-chloro-2-methylbutane with water CH,CH(CH,)CHCICH3 +…

A:

Q: 1) Mg, Et,0 2) O CI Ph 3) H30* 4) H2SO4 5) O3 then CH3SCH3

A: In this reaction at the end we get ketone and aldehyde as a product of the reaction. And here h3O+…

Q: 3. Write the product and the mechanism for reaction: AICI3

A: Ketones can be defined as the organic compounds that contain carbonyl group in a compound.

Q: 6. Redraw these molecules and identify the active atoms by circling them. re 7. Explain in words…

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Q: reaction has a ΔSsystem < 0

A: Entropy is defines as the degree of randomness or may be defines as disorderness. Entropy of…

Q: The elimination reaction between 2-bromobutane and NaOCH2CH3 gives two organic products.  Draw a…

A: 2-bromobutane reacts with sodium ethaonide to give two elimination [E2] products.

Q: An experiment was carried out by reacting cyclopentanone and water in the presence of potassium…

A:

Q: Complete the reactions below.

A: a)  Cyclohexanone is a Ketone.  In ketones carbonyl carbon is electron deficient, hence ketones…

Q: Redraw and complete the diagram below to illustrate nucleophilic attack by the N7 atom of a guanine…

A: Substitution reactions are those in which one group substitutes (or replaces) another group.…

Q: Provide all structures and steps for the following series of reactions. C,H;CH,OH PCC BRCH CO,Et, Zn…

A:

Q: CH3 HI H3C-C-OH CH3

A:

Q: The reaction is Ammonium molybdate and Sodium thiosulfate Molybdenum [Mo7024]^6- Mo04^2- what is…

A: Since you have asked multiple questions, we will solve the first question for you. If you want any…

Q: OH %3D II a) I b) II c) II d) None of the above

A:

Q: 1. Br,, hv 2. МеОK, MеOН, Д 3. OsO д, ру 4. NaHSO, OH %3D + Enantiomer III CO,H IV

A: The reaction given is,

Q: HzS 04 + 2 NH4 Br >2 Br t INH4)2 S04 + 2 HzO 2 AOH +

A: Here , side reaction is E1- Elimination this reaction occurs in two steps . But-2-ene is the side…

Q: Illustrating with reaction mechanisms, show how compounds [1], [2], [3] and [4] are formed.

A: Illustrating with reaction mechanisms, show how compounds [1], [2], [3], and [4] are formed.

Q: Which of the following would not be an appropriate intermediate for a Wolff-Kishner Reaction. NH NEN…

A:

Q: Provide the structure of the major organic product in the reaction shown below. 5. Br 1. Mg, Et20 2.…

A: Grignard Reaction is an organometallic reaction in which different alkyl, aryl-magnesium halides add…

Q: OH

A:

Q: a. Br CH,ONa Br2 CH,CO,H Light NaOH/H20 0H HO.

A: The correct answer is given below

Q: ihe diagram below shows two synthetic pathways by which the compound W might be prepared. C3H;OH…

A:

Q: H2 1. Вн/THF A В Lindlar 2. Он, Н-О2, Н,0

A:

Q: 1) E PB13 Mg, ether 2)H3O* OH F G 1) Co H2CrO4 2)H3O* E

A:

Q: 4. Tryptophan can also form adducts with arenediazonium ions, although the reaction is not…

A: Here the chemical reaction is:

Q: flavor

A: If Compound contain better leaving group like OTs, OMs, OTf, Br, Cl, I etc then it's can easily…

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.