+ H

Q: с o Br Br Br Br o o Br

A: As per Bartley guidelines, and expert is allowed to answer first three subparts of a question.…

Q: Propose a possible reaction mechanism for the following transformation. Draw out the steps with the…

A: In a nucleophilic substitution reaction, the electron-rich species attacks the electron-deficient…

Q: CI A B C D H₂O pyridine pyridine (CH3CH2)2NH 1. SOCI₂ 2. (CH3)2NH, pyridine Ⓒ Done

A: Given transformation: We have to find the reagents for this transformation.

Q: Br ÓH end here start here

A:

Q: The reaction of an alkene with diazomethane forms a cyclopropane ring. Propose a mechanism for the…

A: Please go through the below pic for the reaction mechanism.

Q: Но -OH

A: Ketone react with HCN to give cyanohydrin then further hydrolysis to give alpha hydroxy acid

Q: Devise concise syntheses for the following transformations. Clearly show the reagent and product for…

A: The synthesis is shown below We have to give the multi-step synthesis.

Q: Show how to synthesize the following product as the major product starting with 2,2- dimethylpropane…

A:

Q: (a-b) (c-d) (e-f) OH CI CI HORE ? NH pyridine -OH HAM S CI LIAIH[OC(CH3)3]3 1. LIAIH4 2. H₂O+ 1.…

A: Lithiumaluminiumhydride is a reducing agent. It release hydride ion (H-). According to Q&A…

Q: Synthesize the products by drawing out reagents and intermediates along the way.

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

Q: OCH3 NH, OCH3

A:

Q: e major product for each reaction. OCH 3 O CI & Br2 FeBr3 Caf Cat H₂SO4 SO3 H₂SO4 Cast CH3 Br sogt…

A:

Q: 6. 7. H₂C Br CH3 :0 (CH3)3C-OH NaOH H₂O 2

A:

Q: how to synthesize the final compound from the following starting materials

A:

Q: HO HO `NH2 HO CH3 CH3

A: Various reactions are carried out for the mentioned transformation like oxidation, reduction,…

Q: c. (super challenge for the super motivated). Pay attention to 13C labeling. Åke C13 CN CH 3 EtO…

A: Given reaction :

Q: b. H3C CH3 H3C CH3 steps H

A:

Q: The following synthesis requires more than one step. Specify the reagents you would use to carry it…

A: To Solve this problem we have to complete the given reaction using the given reagents .

Q: (i-j) NO2 (k)

A: In the first reaction, the amide is reduced into amine which is converted into quarternary ammonium…

Q: 10. Propose a mechanism for the following transformation: О H₂O+ (е) НО ОН

A: In the above given transformation a cyclic ester (lactone) is treated with acid in water, this type…

Q: from

A:

Q: Show how to convert the given starting material into the desired product. Note that some syntheses…

A: Cyclohexane on reaction with chlorine in the presence of sunlight or U.V.light gives…

Q: Provide the reagents and mechanism for each step of the synthesis.

A:

Q: Na2Cr2O7 A H2SO4, H2O

A:

Q: 2. propose a mechanism for the following transformation. 1) Excess MeMgBr HO 2) H₂O OH

A:

Q: но 3 но но Tamoxifen

A: Reagents and reaction conditions for each step

Q: I ΖΗΝ,

A: The question is based on the concept of organic synthesis.We need to synthesize the product using…

Q: Draw reaction mechanisms with all reactants, arrows, intermediates, and products. Your mechanism…

A: The objective of this question is to illustrate the reaction mechanism of 4-methylcyclohexanol with…

Q: (a) (b-c) (d-e) (f-g) (h-i) (j-k) (l-m) (n-o) (p-q) (r-s) (t-u) FeBr3, Br₂ CH3 i AICI, NBS CC14,…

A: #(a):  Br2/FeBr3 add -Br group to a benzene ring.  Since -OCO-R (Ester) group is an activating…

Q: The following synthesis requires more than one step. Specify the reagents you would use to carry it…

A:

Q: II NO₂ III NH₂ IV CN VI H NH₂

A:

Q: насна CH3 R., CO₂Et CO₂H 5 mol% dioxane, RT EtO₂C NHR O CH3 H

A:

Q: „NO2

A: According to Q&A guidelines of Bartleby, we are supposed to answer only the first question out…

Q: b. HO,

A: The following compounds can be synthesized by the following reactions: