What reagents (A-D) are needed to carry out each reaction in the following sequence? A в O2N `SO3H H2N° SO3H

Q: . onow how to carry out each of the following conversio reagents you want. Draw the product after…

A: We can use m-CPBA for epoxidation of alkene.

Q: Draw a stepwise mechanism for the following reaction. (Hint: Two Michael reactions are needed.)

A: Given reaction:

Q: What crossed Claisen product is formed from each pair of compounds?

A:

Q: Propose a mechanism and predict the major product. Cl2 hv

A: The reaction between alkanes and Cl2 in presence of light i.e hv is known as chlorination reaction.…

Q: What is the major product of the following reaction sequence? KOC(CH CH2N O a. Ob. Od. ** I

A: In this question, we will see the correct major product for this reaction sequence.  You can see…

Q: Draw the products of each reaction. CH2CHCI2 NANH2 NANH2 c. CH3-C-CH,CH3 а. (2 equiv) (excess) CH3…

A: (a)   (b)   (c)   (d)

Q: Although a Wittig reagent can be prepared from 5-bromo-1,3-cyclopentadiene in the usual way, that…

A: (a)

Q: What crossed Claisen product is formed from each pair of compounds?

A:

Q: Draw a mechanism for the following reaction: H,C CI CH3 HCI |

A:

Q: What starting materials are needed to synthesize each compound by a crossed Claisen reaction?

A:

Q: Draw a stepwise mechanism for the following reaction, which results in the synthesis of bisphenol F…

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

Q: What acetylide anion and epoxide are needed to synthesize each compound?

A:

Q: What crossed Claisen product is formed from each pair of compounds?

A: a.

Q: What is the major product of the following reaction sequence? R = cyclohexyl. Br + Mg ) H2CrO4…

A: The reaction taking place is given as,

Q: 8. Draw a plausible mechanism for each of the following transformations: -OH for conc. H₂SO4 heat a.…

A: Short explanation : Conc. sulfuric acid is donate its proton to alcohol and formation of…

Q: Devise a synthesis of each compound from cyclopentane and any other required organic or inorganic…

A: Since you have posted a question with multiple sub-parts, we will solve first three subparts for…

Q: What is the best choice of reagent to perform the following transformation? Br a. H2SO4 b. H20 с.…

A: We have given one reaction in which removal of br take place and alkene if formed. This reaction is…

Q: 4. Identify the reagents necessary to accomplish each of the following transformations. а. b. Et CH3

A: This is the one kind of nucleophilic substitution reaction in carbonyl carbon .

Q: What is the major product? Draw a mechanism to show how it forms. H2SO4 ETOH H2SO4 H20

A:

Q: Draw the products of each reaction.

A: (a) The reaction of alkene with N-bromosuccinimide in presence of light results in the formation of…

Q: Which reagent (A) would perform the following transformation? 1. ΕίNH (2 equiv.) 2. LIAIH4 A Ph NH2…

A: The answer of the above question is given in step 2

Q: Select the correct set of reagents to carry out the following transformations: НО. HO, ОН A D CI

A: In this question, we want to findout the A, B, C and D Reagents by using mechanism for each cases.…

Q: Quèstion 4 All SN2 reactions proceed with backside attack of the nucleophile. When nucleophilic…

A: In SN2 reaction when a nucleophile attacks on chiral carbon atom then inversion of configuration…

Q: What starting materials are needed to prepare each compound using a Michael reaction?

A: The reaction in which an enolate ion of one carbonyl compound undergoes conjugate addition reaction…

Q: 8. 1. HBr (1 equiv) 2. HCI (1 equiv) A) Br Br B) CI Br C) D) Br E) None of these choices. What is…

A: The given reaction is;

Q: 1. HBr (1 equiv) 2. HCI (1 equiv) Br A) Br B) CI Br C) D) - Br E) None of these choices. What is the…

A: Answer is explained below.

Q: Predict the major product or reagent that completes the transformation

A:

Q: What is the best choice of reagent(s) to perform the following transformation? ОН O H20, H2SO4 O…

A:

Q: Which reagent in each of the following pairs is more nucleophilic? a) (CH3)3B and (CH3)3N b) H2O…

A: The reagent has a negative charge or lone pair of electrons acts as a nucleophile. As the…

Q: Draw the products of each reaction, and state whether the reaction is fasteror slower than a similar…

A: The products of the above reaction and the reaction is faster or slower than a similar reaction with…

Q: (def) Predict the major product or reagent that completes the transformation

A: The question is based on the concept of organic reactions.   We have to identify the product formed…

Q: Which enol will undergo tautomerization most slowly? A B OH Ме. Me Но- Ме Ме Me O A O B ос

A: 1) The enol that will undergo tautomerization most slowly is

Q: Which is the correct order of reactivity towards a nucleophile, from most reactive to least? H3CO F…

A: Given compounds:

Q: Draw the products of the following reactions w given starting material 4. NaNH2 followed by CH3CH2Br…

A: When alkene is treated with sodium amide , removal of proton takes place. When this treated with…

Q: Draw the products of each attached reaction.

A: NBS is a brominating agent. It adds Br to the allylic position if there is a radical initiator.

Q: Draw a stepwise, detailed mechanism for each reaction.

A:

Q: Draw the major product for each reaction. HNO3 H,SO4 O,N fuming H,SO4 NO2 OMe CI AICI3

A: Note: As per company norms we can answer only 3 subparts. Please share rest of the parts as a…

Q: Part A What is the major product formed when the following compound undergo an E1 reaction? CH, CH…

A:

Q: Draw a stepwise mechanism for the following reaction, which results in the synthesis of bisphenol F…

A: The organic reactions help in the synthesis of various new organic compounds.

Q: Q10) Explain how to obtain A and B as major products in the following transformations with suitable…

A: Organic reaction mechanisms.

Q: 3. Draw the products formed when each compound is treated with HNO 3 and H2SO4. State whether the…

A: Concept is based on Nitration.

Q: What is the best choice of reagent(s) to perform the following transformation? O 03; followed by…

A: To solve this problem we have give the reagents which gives the desired product .

Q: Give the major product from A-E Give the major product trom A-E. the HBr D H2O2 H2 A Ni Ch H/H2O E C…

A: Different reagents are used for the synthesis of a compound (product) from the different compounds…

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

A:

Q: HO CH3 d Но a CH3 CH3 Но e

A: Grignard reagent is RMgX where carbon is attached to a magnesium halide. Reaction of Grignard…

Q: Draw the enol form of each keto tautomer in parts (a) and (b), and the keto form of each enol…

A: Keto-Enol tautomerism is an equilibrium that exist between carbonyl group (aldehyde and ketone) and…

Q: What is the major product for the following sequence? A A X B В Your answer C D D 1. HBr 1.…

A: In step first there is overall elimination reaction and most substituted alkene formed. In step 2…

Q: Which compound undergoes the fastest nucleophilic acyl substitution? A. B. H3C D. С. O,N O,N NO

A: In nucleophilic acyl substitution reaction, a nucleophile attacks the C atom of -C=O and removes the…

Q: Draw a stepwise, detailed mechanism for the following reaction.

A: The CH3NH2 attacks on the Cl and removes it in step 1. And then in step 2, due to presence of…

Q: What is the best choice of reagent(s) to perform the following transformation? ÓH a. H20, H2SO4 b.…

A:

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.