Predict the products of the following reactions. ) trans@2,3@epoxyoctane + H+, H2O

Q: Predict the products of reaction of pent-1-yne with the following reagents. ) H2, Pd>BaSO4,…

A: Concept Introduction  Hydrogenation of alkynes with Lindlar's Catalyst  Barium sulphate coated with…

Q: What products would ypu obtain from reaction of 2,4-dimethyl-2-pentene with BH3, followed by H2O2,…

A: Alkene reactions with BH3 and H2O2 in presence of base are Hydroboration oxidation reaction.

Q: mC PBA,

A: The Baeyer–Villager oxidation is an organic reaction in which ester formation takes place from…

Q: In synthesis shown in box, which of the following reagents is expected to give the indicated pro 1.…

A: Esters can undergo hydride reduction with LiAlH4 to form alcohol.

Q: Provide the major products for the following reactions?

A: in nucleophilic substitution reaction nucleophile attacks on electophilic center and form  new…

Q: to Cis-allvere H3CO

A:

Q: MeO MeO. OH 5.0 eq. Li, ETOH HO. liq. NH3 MeO OMe OMe

A: In presence of Li/ liq NH3 or Na/ liq NH3 benzene undergoes birch reduction. Due to birch reduction…

Q: Predict the major product of attached epoxidation.

A: Sharpless epoxidation is an enantioselective reaction that prepares 2,3-epoxy alcohols from primary…

Q: Exl. OH Ph ) Ho A Ph KH,18-c-4, THF, (i) 2) NO2 Xylanes, hat NO2

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Q: Propose reagent(s) or product(s) for the attached transforamtion

A: The reaction given is,

Q: Please, Predict the major product of the following reactions Please give answer all questions

A: a) The first reaction depicts the hydration of ketone. When water is added to ketone in presence of…

Q: 9. Draw the structure of product, substrate or condition in the following reactions (should clearly…

A: The products formed during the reaction depends upon the substrate and the reaction condition. All…

Q: H3C

A: Detail synthetic pathway is given below

Q: Br2, H20 c) Ме HI d) F3C н он e) Br Br2 f) Br

A:

Q: Show the structures of alkenes that give the following products on oxidative cleavage with KMNO, in…

A: The oxidative cleavage of alkene takes place in the presence of KMnO4 in the presence of acid to…

Q: UV + Br2

A:

Q: Predict the major and minor products for the following reaction. OTS ? NaOE

A:

Q: How would you carry out the following reactions

A: Please note- As per our company guidelines we are supposed to answer only one question. Kindly…

Q: Predict the Product of the reaction and indicate regiochemistry and stereochemistry when relevant.…

A: An alkene gets converted to viccinal diols(1,2-diols) in presence of OsO4. The stereochemistry of…

Q: Predict the major products of the following reactions. ) p-ethylbenzenesulfonic acid + HNO3, H2SO4

A: Given, p-ethylbenzenesulfonic acid + HNO3, H2SO4

Q: Predict the productiss of the tollowing ucleophilic Substitutioan 1. reaction: Br +H20 ->

A:

Q: 1. (CH3CH2),CuLi 2. H20, H*

A: [As per rules only first question could be answered]   Organocuprate, a soft nucleophile, preferably…

Q: otherwise indicatec provide the major organic products of the reactions. Please inciude…

A: Note: According to our guidelines we are supposed to answer only first three subparts. Kindly repost…

Q: Provide the product for the following reaction. HO SOCI, pyridine HO OA

A:

Q: Name the products for an SN1 reaction with iodide for the following compound. Indicate major and…

A: for Sn1 reaction-  1st step remove the leaving group, and formation the carbocation 2nd step…

Q: Be the product of the reaction scheme below? TosCI NaNH(CH3) pyridine DMSO Na ONa

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

Q: Show the mechanisms for the following reactions. Show all movement of the electrons. Do not skip or…

A: The first reaction is the addition of DCl to 2,4-Hexadiene. The first step involves in the reaction…

Q: The synthesis shown below generates an achiral product from a chiral starting material. Provide the…

A: The product formed from the given reaction is,

Q: CH3CH2OCH,CH3 LIAIH4

A: The reaction is as:-

Q: HCIO4 Br2 MECO2H

A: 1- In the first reaction, Keto form converted into enol form in acidic medium and then enol form is…

Q: Farnesyl pyrophosphate forms the sesquiterpene shown here. Propose a mechanism for its formation.

A: The pyrophosphate in farnesyl pyrophosphate gets cleaved by the attraction of shared pair of…

Q: Predict the product 1. KOtBu A Me Bri Ph. 2. Cl₂, MeOH Me Please let me know the detailed process…

A:

Q: Predict the major product of attached epoxidation.

A: Given reaction,

Q: 1. Propose a mechanism and predict the product. 1. LIAIH4 2. H20 1. PPH3 Br 2. nBuLi 3. 1. LIAIH4…

A: Given, We have to predict the product along with the mechanism.

Q: Perform the following retrosynthesis. OH NO2 NO, он Он

A: The answer for first question is given below. Kindly repost the other question as separate one.

Q: Show the mechanism for the nucleophilic aromatic substitution below. Br NH2 NaNH, ZON NaBr ZON

A:

Q: 2. Predict the major product(s) of the following reaction sequences. 1. I, NaOH (excess reagents),…

A:

Q: redict the major product(s) of the following reaction sequences. 1. I2, NaOH (excess reagents), CH3…

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

Q: Give mechanisms to explain the outcome of the following sequence of reactions, remembering to…

A:

Q: Predict the product formed when the compound shown below undergoes a reaction with MCPBA in CH,CI,.…

A:

Q: Name the products for an SN1 reaction with iodide for the following compound Indicate major and…

A: here, Sn1 reaction is given condition of Sn1 reaction- 1. remove the halide ion and formation of…

Q: Place the following in order of reactivity towards electrophilic aromatic substitution. NO COCH, OH…

A: Aromatic electrophilic substitution reaction: Aromatic electrophilic substitution reactions are the…

Q: Propose a mechanism for cach of the following reactions ОН H2SO4 + H2O ОН

A: This reaction is the dehydration of alcohol by the formation of carbocation as intermediate. Hence…

Q: Give the major product(s) of the following reaction. TSCI CH3CH2OH pyridine

A: This reaction shows tosylation of alcohols and alkyl tosylate has been formed as product.

Q: Provide a plausible arrow pushing mechänism fof the ОН OMe TSOH, H20 OMe

A:

Q: Br 3. HCI, H2O

A: First reaction with Mg it will form grignard reagent after this  CO2 reaction will give carboxylic…

Q: I. Draw the structure of the main product of the following Deactions. Include stereoshemistry, in…

A:

Q: Predict the major product for the following reaction including steree OH

A: We have given that  It is an diels alder reaction.  In the Diels–Alder reaction a 1,3-diene reacts…

Q: What substrate below is ideal for SN1 reaction?

A: Following are the appropriate answers of the given question.

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.