uestion Desarrolla una posible ruta de sintesis: (escribe solo los reactivos utilizando el teclado y coloca los numeros sin utilizar subindices inferiores; Ejemplo: 1) Br2, H2O; 2) H2SO4, H2O Br NO2 只i

Q: СЕЗ CF3 NaBH4 CH3OH What is the product? -OH is endo or exo? Why?

A: Exo/Endo attack: The attack of nucleophile through the axial or equatorial position, depends upon…

Q: a. b. C. HBr Cl₂ 1) BH3, THF 2) H₂O₂, OH-

A: a) HBr adds to propene according to Markonikoff's rule. The rule states that the negative part of…

Q: A synthesis of the pain reliever phenacetin is outlined in the following equation. What is the…

A: The given compound is Phenacetin. It can be synthesised from p-Nitrophenol.

Q: Below is a short reaction sequence. Provide the structure of the two missing organic compounds. NaOH…

A: If the base is alc.NaOH then it undergoes elemination reaction results in the formation of highly…

Q: 2

A: The given reaction is aromatic electrophilic substitution reaction.Explanation:This reaction is…

Q: Write the necessary reactants in the following reactions

A: A question based on introduction to organic chemistry that is to be accomplished.

Q: Draw the structure of the major organic product(s) of the reaction. CI 1.2 CH3CH₂CH₂MgBr, ether + 2.…

A: The above given reaction is an example of Grignard reaction with acid chloride.  The reagent…

Q: b.) ECO 1) CH3CH₂CH₂ Bv 2.) H30+ OEt 1.) NaOEt, EtOH 2. HCI

A: Organic Reactions are given.We have to make the products.

Q: 1. 9-BBN 2. H2O2 NaOH

A:

Q: Calculate the volume of 1 M CoCl2 needed to prepare 100 mL of 0.25 M CoCl2

A: Molarity of solution 2 (M2) = 0.25 Volume of solution 2 (V2) = 100 ml Molarity of solution 1 (M1)= 1…

Q: Choose the reaction conditions to complete the acid-base reaction shown. A: CH3CO2H B: NaOH, H2O C:…

A: For the acid-base reaction of isopropyl alcohol to result in the formation of propan-2-olate the…

Q: -Et 1) ВН;:THF 2) H-О2, NaOН

A:

Q: Draw the major product of this reaction. Ignore inorganic byproducts. 1. B2H6, THF 2. H₂O2, NaOH

A:

Q: Indicate the major organic product that would be formed under the conditions below: 1. ВН3 THF 2.…

A:

Q: Major product

A:

Q: О COOH Br OCH(CH,); en ОН NO₂ NO₁₂ (h) CH,OCH,CH,

A: Rules for IUPAC nomenclature of organic compounds:According to IUPAC, the nomenclature of compounds…

Q: USE THIS OH MAKE THIS

A: N-phenylpropionamide is a degradation product and potential biomarker of smoked Fentanyl with toxic…

Q: Draw the major organic product for the reaction: Br NaCI H20

A: Given,

Q: Draw the structure of the major organic product(s) of the reaction. CI OH

A: Draw the structure of the major organic product(s) of the reaction.

Q: NH2 major product?

A:

Q: 10. Provide the product of the reaction.

A: These reactions undergo through two steps     Step- 1. Formation of carbocation     Step-2 .…

Q: OH 1) NaH 2) 9 3) H20

A: We have to predict the product of given reaction.

Q: 1. BH 2. Н2О2, NaOН CECH С — Н 2.

A: Electrophilic addition reaction takes place when borane reacts with alkene or alkyne. Now peroxide…

Q: ii. Which is the major product of this reaction? Ph OEt 1) 2 eq. PhMgl 2) H3O+ OH Ph Ph. OH Ph

A:

Q: 8. Provide structure(s) for the starting material(s), reagent(s) or the major organic product(s) of…

A: LiAlH4 is a strong redicing agent that reduces ester to primary alcohol and ketone to secondary…

Q: Which reaction will give butanoic acid? A) B) C) D) Br 1. CH3MgBr Na₂Cr₂O7 2. H₂O NaCN Br Mg all of…

A:

Q: 1. Hg(OAc), EtOH 2. NaBH4, NaOH A) B) C) но. + CO2 D) E)

A: In presence of Hg(OAc)2 , EtOH followed by NaBH4 reduction ,oxymercuration - demercuration reaction…

Q: Provide an IUPAC name for each of the compounds shown. (Specify (E)/(Z) stereochemistry, if…

A: The given compounds contain an alkene functional group. For the IUPAC name of an alkene, first of…

Q: 14. What is the main product of the reaction shown below? COOH COOH OH ONa A OH OH NaOH H,O COOH B…

A:

Q: What are the products of the following reaction?

A: Ketones reacts with ethylene glycol in the presence of HCl to give a cyclic product named as…

Q: Draw the major organic product for the reaction. 애 ㅇ c Hz CrOusy

A: The reaction is an example of oxidation of alcohol.The secondary alcohol on oxidation with H2CrO4…

Q: NaOH A FeCl3 1. NANH2 B 2. CH3BR C

A: When benzene is reacted with Cl2 in FeCl3, Chlorobenzene is formed.

Q: Indicate the major organic product from the reaction shown. 1. Li 2. B(OCH33 3.Pd(PPH3)4 NaOH Br Br-

A:

Q: i. Eto, EtOH ? ii. H₂O iii. DIBAL-H (-78°C)

A: Step 1:  *EtO⁻, EtOH*: This is a base (ethoxide) in ethanol, which can deprotonate a hydrogen from a…

Q: (a) 1. NBS, hv 2. NaOH, H₂O 3. CHBr3. (CH3)3COK*

A:

Q: Provide the major organic product of the reaction shown below. H₂C HỊCH, CÓ CH₂ OCH₂CH₂ H₂O*, A

A: In presence of H2O /heat and acidic medium Acetal can break and form carbonyl compound.

Q: CN you Na,Cr,07 H2SO4, heat HO

A: (1) when 2-ethylbutane nitrile is treated with water Molecules then initially trihydroxyl group…

Q: What is required to complete the following reaction? H₂ H₂C CH₂ O 1) MCPBA 2) HCI O 1)NaOH 2) HC1 O…

A: MCPBA is meta-chloroperoxybenzoic acid.  It forms epoxide when react with alkene.

Q: KO'Bu BUOH b) 1. Na°, lquid NH 2. Cl H0 1.0

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

Q: Complete reaction

A: Jones reagent consists of an oxidizing agent, an acid, water and the acetone. Jones reagent is used…

Q: 1. CH₂CO3H 2. ETOH, H* ?

A:

Q: i) j) OH k) 1) ОН H₂SO4 OH TSOH TSC OH pyridine HBr m) n) o) OH он л он НI POCI3 OH SOCI₂

A:

Q: Carboxylic Acid Derivatives Resolve the reactions.

A: Acetic a hydride with ammonia gives amide.  Lactum with lialh4 gives amine and alcohol

Q: HạC NH,

A:

Q: estion Draw the most stable conformation of ethylcyclohexane. Show every bond to hydrogen. Clearly…

A: The most stable conformation of a cyclohexane is chair form with all the substituent at axial or…

Aldehydes and Ketones

Aldehydes and ketones are organic compounds that have a carbonyl group, C = O, as their functional group. They both differ in the placement of this carbonyl group in their structures.