Predict the product of the following reaction:

Q: D. CH,CH;CH,CH, + O +02

A:

Q: sec-butyl bromide + Li/Cul→ A 2-methylbutane + C2 (in uv light) → B isobutyl bromide + Mg/ether → c

A: Given,

Q: „CONH2 1. LIAIH. 2. HyO CH3 CH3 1. LIAIHA b. H2C=CHCHCH,CO,CH, 2. HgO**

A:

Q: Predict the major product of the following reaction:

A:

Q: (13) 14 (15) 애 애 1. NaHCO3, H2O 2. H+ 애

A:

Q: 1. NBS 2. он PBr3 Ether

A:

Q: Predict the product(s) of the following reactions:

A: The alkenes on ozonolysis lead to the formation of two carbonyl compounds. Depending upon the…

Q: 1) Predict the major product(s) of the following reactions: CO₂H HNO₂ ? H₂SO OCH₂ CH₂CH₂CH₂Cl AICH

A:

Q: 1. NaOMe 2. LIAIH4 3. H20 (workup) `NH2

A: Amides gives no product with sodium methoxide (NaOMe). The nucleophilic attack of ethoxide results…

Q: SOCI, or P205 or POCI3

A: Predict the product of the following:

Q: Predict the major product of the following reaction:

A: The question is based on organic reactions. We need to identify the product and explain its…

Q: m. n. CN NH₂ 1. (CH3)2CHMgBr, ether 2. H3O+ SOCI2

A: The question is based on organic reactions. we need to identify the product formed in each of the…

Q: NaOMe/MeOH Br

A: Given reaction is an example of E2 elimination reaction where base abstracts a proton from a group…

Q: Predict the product(s) for the following reaction

A:

Q: LOH 1. NaOH 2. CH;CH2B H2 C0-CH3 H2 HBr o-CH2 CH heat, 250 °C CH2 HCI H3C, Ether

A:

Q: Please predict the product for the following reactions

A: The given reactions are shown belowWe have to predict the product of those reactions.All the given…

Q: g. h. i. H₂C H O ОН 1. KMnO4 2. H3O+ ОН CrO3 H3O+ 1. (CH3)₂CuLi, ether 2. H3O+

A: The question is based on the concept of organic reactions. we need to identify and explain the…

Q: Predict the product(s) of the following reactions:

A: Since you have posted questions with multiple sub-parts, we are entitled to answer the first 3 only.…

Q: Predict the major product of the following reaction:

A: When morpholine combines with an alkyl bromide, it usually undergoes a substitution…

Q: CO2CH2CH3 1. CH3CH2MgBr 2. H30+ a. CH3 1. DIBAH CH3CHCH2CH2CO2CH3 b. 2. H30+ .CONH2 1. LIAIH4 2. Нао…

A: Observing the given reactants shows that the given reactions are nucleophilic acyl substitution…

Q: 1. NANH2 2. CH3I B 3. Na, NH3

A:

Q: 1. EtMgBr 2. H30* 3. NaCN 4. H3O*

A: Grignard reagent react with keto group and gives 3° alcohol then further NaCN will react with alkyl…

Q: DME [0] · A== heat dne DME heat DME heat

A: Given first three reactions are Diels-Alder reactions.Diels-Alder reaction is [4+2] cycloaddition…

Q: 1.2 eq EtMgBr 2. HBr, heat CI

A: Grignard regent is addition reaction in which ethyl group carry negative charge and MgBr has…

Q: Br 3. HCI, H2O

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

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.