но NH2 но HO mild H+ HO 1. КОН -OH. H,0 HN CI

Q: The reactivity of the below compounds towards nucleophiles is: R CI NH2 OR a O a. b>cod a Ob. acd» b…

A: The derivatives of carboxylic acid are derived by the replacement of OH group of carboxylic acids,…

Q: Predict the major product of the reaction show below. H3O* / H2O heat JDHDMC HO. OH HO HO. HO HO ÓH

A: Given reaction:

Q: OH RCOCI „NH2 EtO OEt A Base H,0*

A:

Q: 1) Propose an efficient synthesis for the following transformation: + en Br Koty .2 HO Br Hz S04…

A: Organic synthesis of a specific molecule requires a specific amount and type of reagent . It's not…

Q: (a) CO2H 1. SOCI2 2. PHCH,OH, pyridine (b) N 1. LIAIH4 2. H* /H2O

A: The given reactions are represented as follows:

Q: OH H30* он

A: To show the mechanism of the following reaction

Q: Give the major product(s) for each step of the following sequence of reactions: a) HO HNO3/H2SO4…

A:

Q: a. Propose a stepwise mechanism that accounts for the transformations below. 1. NaOEt/ELOH 2. H,O+,…

A: Organic reaction mechanisms

Q: 3) Draw a plausible mechanism for the following transformation: 0. 0. H³0Ⓡ NO₂

A: In this question we have to tell the product of the reaction and also its mechanism.

Q: Which of the following is the major product of the following reaction sequence? NBS 1) Mg. ether…

A: Allylic halogenation:N-Bromo succinimide is the best reagent for an allylic halogenation reaction.…

Q: 1. Propose a mechanism to rationalize the following transformations. TSOH a) HO H2SO4 THE b)

A: Mechanism of organic reaction.

Q: Show the major organic product and mechanism for the transformations below.

A:

Q: the and retrosynthesis corresponding forward reaction for the following compounds : OH 3. (a)…

A: Retrosynthesis: It is the phenomenon of breaking down the specific molecule into immediately present…

Q: d. Please predict the major product only here. No need to show the mechanism again. xs H20 65°C,…

A:

Q: Propose an efficientsyntnesisfor each of the following transformations: NH, NH2 1. NH2 2. 3. Drawthe…

A: 1. At first aniline is converted into 2,4,6-trichloro aniline on reaction with Cl2/H2O. Then it is…

Q: 2. (a) Predict the products of the following reactions with mechanism : to DCC Ti) H3C- -COOH →?…

A:

Q: 3. Complete the following reactions by giving products in each case. KMNO4 H. 1) LIAIH, 2) H3O*…

A: 1-KMnO4 is oxidizing agent. 2-LiAlH4/H3O+ is reducing agent . 3-alcohol when react with aldehyde in…

Q: A student attempted to brominate the double bond in pent-4-en-1-ol, but ended up with the following…

A: The nucleophilic substitution reaction involves the attack of the nucleophile on the carbon bonded…

Q: What is the major product and the mechanism for the reaction of shown below? Br H3C OH CH3 HO CH3…

A: The correct option is compound C/ SN1

Q: What is the major organic product obtained from the following sequence of reactions? Br (CH3)3COK…

A:

Q: 3. Draw a mechanism for the following reaction. A) HOʻ 1. СH;CH-MgBr 2. H3O* HO B) 1. но |H,8o| H.…

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

Q: (e) Provide a reasonable mechanism of the following reaction .CI OCH3 CH3ONA Ether (5) (c) Show how…

A:

Q: 3. Propose a plausible mechanism for the following transformation: OH

A: Organic transformation in acidic medium:

Q: Determine the major product and provid- Oraw a plausible mechanism for the reaction shown below.…

A: Sodium borohydride and lithium aluminium hydride both are hydride ion transfer reduicng agents but…

Q: 4. The following reaction occurs through an Elcb mechanism followed by a tautomerization. Provide a…

A:

Q: (c) Predict the product(s) for the following reaction with supporting mechanism. i) SeO, Aq. dioxane…

A: This ragents are oxidizing agents.Oxidation takes place with DDQ and SeO2.

Q: please show the detailed mechanism for each step for the reaction below. OTBDPS Me TMANO (anhydrous)…

A: Step 1 : alklyne addition to two coblat atoms. Step 2 : olefin addition to one of the coblat atom.…

Q: The major product of the following reaction is an alcohol. Which of the following best describes…

A: Ans

Q: 1. Predict the major product(s) of the following reactions: CH3CH2CI AICI3 (a) CH3CH,COCL AICI3 (b)…

A: 1(a) The reaction is a example of Fridel Crafts alkylation.  (b) The reaction is a example of Fridel…

Q: 3. Propose a mechanism and predict the product. Include any relevant stereochemistry. a) HCI b)…

A: a) Alkenes react with HCl and undergo addition reaction via carbocation formation mechanism. Since…

Q: CH,COCI AICI3 NH2NH2 KOt-Bu DMSO MeO. MeO Et MeO Me А B `NH2 MeO. MeO. `Et CI C D

A: We have to predict the major product.

Q: Analyze the following reactions. Draw the major product of the reaction and state the mechanism…

A: A. tBuOK/tBuOH forms a strong base. Br is a good leaving group. Hence, here E2 elimination reaction…

Q: er: HBr CH3 CHa CH2 CHa Br CH3 CH2 CH2 CH2 Br + Hao

A:

Q: 1. (CH3CH2)2CuLi H 2. H-О, H'

A: Since you have posted multiple independent questions in the same request, we will solve the first…

Q: Propose a mechanism for the reaction shown below. a) CI OH O NH2 + CI Heat NO2 NO2 b) NO2 HNO3 H2SO4

A:

Q: Predict the major product and show the complete mechanism for each electrophilic reaction below. (a)…

A:

Q: Wnte reaction schemes (no mechanism required) to show how the followin transformations can be…

A: In order to solve this question, we will use reactions like aldol condensation, reduction using…

Q: (a) What happens when CH3—O—CH<sub3 is heated with HI?(b) Explain mechanism for hydration of acid…

A: We are authorized to answer one question at a time, since you have not mentioned which question you…

Q: 3.1 Propose a detailed mechanism for the reaction below: AICI 3 CI

A:

Q: -phenyl- ga) al with the the final Intermediates Draw sequence below along reaction after each step…

A: The crucial intermediate for this given reaction sequence is a carbanion and it reacts with given…

Q: 1. ether 2. H30* H. a)

A: This is the nucleophilic addition reaction of grignard reagent to the carbonyl compound to give…

Q: d) e) of n CI ia AICI3 CF 3- H

A: The solutions are given below -

Q: 5) Provide the products necessary to complete the synthesis below. Indicate what mechanism was used…

A: The above organic transformation is given below

Q: soagain after upeatation thil single -H s Heplaced by- -OH ーH L 12 Be t

A: The detailed solution of your question given below-- We know that the reaction is carried out with…

Q: Select the major product of the following reaction sequence. excess CH;MgBr H;O* (CH;CH,),O OH…

A: Reactions of Grignard reagents are believed to involve an unsymmetrical cleavage of the R-MgX bond…

Q: For the reaction given below, predict which product will be the major one and by what mechanism it…

A:

Q: но осн 1. b. CI CI H DMSO HO, 2. NET3 C. of PPH3

A: Hemiacetal deprotection Swern oxidation Wittig reaction

Q: a) HO OH from b) H3C, OH

A:

Q: 2:3. wotte reachon scherme ( no med 15 sequiredl and shues केर डिा9 Followng huw can be affeesed,…

A: The transformation of the following reaction needs to be determined.

Q: Reaction of benzylmagnesium chloride with formaldehyde yieldsalcohols N and P after protonation.…

A:

Designing a Synthesis

Organic synthesis is a branch of chemical synthesis that involves the planned construction of organic compounds/molecules from smaller units that possess functional groups. Friedrich Wöhler was the first scientist who designed the synthesis of an organic compound, urea from inorganic starting materials silver cyanate with ammonium chloride via a simple, one-step synthesis.