NaOH CH ethanol / H,0 NO2 NO2 Chalcone 3-Nitrobenzaldehyde Acetophenone

Q: NH2

A: The given reagent is Di-tert-butyl dicarbonate which is commonly known as Boc anhydride. It is a…

Q: Detailed reaction mechanism:

A: The explanation is given below-

Q: Mechanism 1. Provide the complete mechanism for the reactions below. You must include appropriate…

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Q: CH, CH, H,C- -CH H-C O a SN1 O b. E1 Oc SN2 Od. E2

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Q: CI- NaOH, 100 °C ?

A: The bimolecular nucleophilic substitution reaction takes place.

Q: Describe a sequence of reactions for the following reaction. A) 1) CH3CH₂O-, EtOH; 2) BH3/THF; 3)…

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Q: Suggest a synthesis of ketone 6 from (E)-3,4-(dimethoxy)cinnamic acid 9. You can assume that any…

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Q: ju ja -> Cs H₂ NO + нсе

A: Molecular formula=C5H9NO HDI = (2C+2+N-H-X)/2 HDI=(2*5+2+1-9-0)/2 HDI=4/2 HDI=2 From HDI =  given…

Q: 10. Convert the followings b) <20 ott c) Describe the mechanism for CH3- the following I (- Nad)…

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

Q: он актиди ноње, наада

A: The given reaction scheme is shown below We have to give the mechanism of the above reaction.

Q: i) PhMgBr ii) H2O

A: The Grignard reagent is denoted as R-MgX, where R can be an alkyl or aryl group and X is a halogen.…

Q: 1. LDA (slight excess) 2. CH3CH2I

A: LDA is a sterically hindered strong base. LDA is the best reagent to synthesize the kinetic enolate.…

Q: Anthracene P(C6H5)3- Xylene at reflux 1.1 equivalent

A: First step reaction is Dieles Alder reaction called [4+2]π cycloaddion reaction between diene and…

Q: F H3C AICI 3 Br

A: The reaction is Friedel-Crafts alkylation of fluorobenzene involves substitution of a hydrogen atom…

Q: Provide the mechanism and product

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Q: Provide the major organic product of the reaction shown below. 1) Н2О, Н.О. А 2) CH CH OH, H.Oº, А…

A: -&gt; In presence of H2O /heat and acidic medium Acetal can break and form carbonyl compound. -&gt;…

Q: C) NH2 CI Br heat

A: Given : To determine the above equation with mechanism.

Q: 1) PhLi Н 2) H3O* NH

A: Since PhLi is a strong base Hence it will remove the H from the reactant.

Q: Predict the product for the following reaction. OH H2SO4 HO,

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Q: e. НО фон нот да H+

A:

Q: H+, H2O

A: Given,the reaction is:

Q: A) B) 1. LIAIH4 CI 2. H30 OH 1. Excess CH3MgBr 2. H3O+ OH CH3 CH3

A: Lithium aluminium hydride is Strong reducing agent it reduces ketone functional group into secondary…

Q: i) CF3CO2H, UV light ii) K2CO3, CH3OH N. CI

A: When a halogen is substituted for the nitrogen atom, it is termed as the N-halogenated amine. The…

Q: CeHgLi

A: Introduction :  We have to tell the product for this reaction .

Q: i. H,C CH3 CH, c-CH CH CH CH H,C CH3 Он Br ii. HO HBr

A: Organic synthesis examples.

Q: NaOEt ELOH CO,Et CO,Et CH;CO,Et

A: The formation of intermediate (1) is shown below.

Q: Draw detailed mechanisms for the following transformations Мео. Br2, NaOH Meo, NH2 `NH2 H20

A: The details solution for this reaction is provided below in attach image.

Q: Provide the reaction mechanism.

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Q: Give mechanism of this reaction ASAP

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Q: Give the reaction mechanism for ETHYNE and bromine solution. Draw and explain the steps of the…

A: Ethyne has triple bond which can give addition reaction .

Q: 10. 9. Br HOC HOC Meo Br 1. Con 12. OH OH 13 14. Br Br Br Br

A: There are several reactions mentioned here involving the participation of aromatic, carbonyl and…

Q: Provide mechanism

A: The required answer is given below Explanation:Step 1: Step 2: Step 3: Step 4:

Q: action. cooH To Itoo ć cood

A: Decarboxylation reaction takes place

Q: CI / NH 1. KNH₂ 2. H₂O Br2, FeBr3 3

A:

Q: Can you show me how the mechanism is done? 1.3 BH₂ THF 2. 3 H₂O₂, 3 NaOH, 3 H₂O

A: An arrow always depicts from a region of high electron density to low electron density ; that is…

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.