1) NaOEt / ETOH 2) H300 +

Q: a) Propose a mechanism for this reaction. Нeat OH H20 200 °C

A: In this question, we have to find out the correct answer of given problem by the help of free…

Q: Provide the missing products in the reaction sequence shown below. You need to show the molecule…

A:

Q: CH,OH /H° ОН ANISM

A: - given compound is the carboxylic acid  Which reacts with the alcohol in presence of acidic…

Q: Propose a mechanism for the following reaction.

A: A mechanism for the following reaction has to be proposed

Q: 1. Show a detailed mechanism for the following reaction. 1. Cl2, NaOH HO, 2. H3O*

A: Haloform reaction :- Formation of carboxylic acid from Ketone in presence of Halide ( Chlorine ,…

Q: Propose a reasonable mechanism for each product in the equations below. OH H2SO4 / H20 HO Br OH Br,…

A: First reaction is the epoxide ring opening in the presence of acidic condition and the hydroxide…

Q: b) Propose a detailed reaction mechanism for the following conversion. он Acetone HCI но но. -OH OH…

A: Acetone /HCl is used for the protection of syn-1,2-diol. For protection with acetone/HCl glucose…

Q: Provide a mechanism for the following transformation: OH Cro3 но. H30*

A: The mechanism of the given reaction is given below,

Q: Propose a detailed mechanism for the following reaction: HO OH H₂SO4 O y

A:

Q: e the best reagents to complete the reaction shown below. NaH A (CH3)2CHCH2CI OH NaH B (CH3)2CHCH2F…

A:

Q: CH3 Na/CH3ОН NH3 (liquid)

A: Given reaction is example of birch reduction.

Q: Provide a step by step mechanism for the following transformation. NH2 N2* HCI, NaNO2 H20

A:

Q: Propose a mechanism for each of the following reactions:

A: (a)The mechanism is given below.

Q: Br CH;OK a) b) Sn1 Sn2 c) d) E1 E2

A: Generally, alkyl halide or alcohols undergo elimination reaction which give rise to alkene.…

Q: (CH3),COCH3 HI (CH3)½CI CH3I + + H20

A: In this question, we have to find out the correct answer of given problem by the help of the…

Q: Propose a mechanism for the following reaction:

A: The given reaction is represented as follows:

Q: Show a possible mechanism for the following reaction 1) LAH (xs) 2) H3O* 3 MeOH

A:

Q: What is the final product of the following sequence of reactions? 1. NANH, CH,C=CH 2. -CH,Br…

A: The Given  When Alkyne reacts with NaNH2 it will from terminal salt of alkyne then after reaction…

Q: Which compound is a major product of the reaction sequence shown below? (1) benzene COOH OCH3 OCH3…

A:

Q: Propose a mechanism for the following reaction H2SO4 CH3-0-H OCH3

A:

Q: NgOH, EtoH. HO (+H20 + NaCI)

A:

Q: What is the BEST way to carry out the following transformation? H. KMNO4/H3O+ ВНз; NaOH/H202 O…

A:

Q: Br 1) NaOH / 70 °C 2) H30° NO2

A: This is aromatic nuclophilic substitution  reaction.

Q: Propose a mechanism for the following reaction:

A: The nucleophilic substitution reaction involves the reaction of the nucleophile to the carbon…

Q: H3CO. NaOH H3CO H3CO OCH

A: An aldol condensation is a reaction in which an enolate ion reacts with a carbonyl compound to form…

Q: What set of reagents can best accomplish the following transformation? OH ? A) Cl₂, hv B) Cl₂ in H₂O…

A: The reagent that can be accomplish in the following transformation is:

Q: 5. Propose a synthetic pathway for molecule X to molecule Y using the reagents boxed below. Note…

A:

Q: Which of the following is the best method to carry out the following transformation? - OH (a) H₂SO4,…

A: We will draw all the product of each reaction.

Q: Draw the final product of this series of reactions. Br 1. 1 equivalent of KOtBu 2. MCPBA 3. H3O*/H2O

A: The reaction given is,

Q: Which compound would be the product of the reaction sequence shown below? MgBr 2. H30*/H20 3. РСС 4.…

A: RMgBr is a grignard reagent and it attacks the carbon attached to double bonded Oxygen atom and join…

Q: 3. Propose a mechanism for the following reaction sequence. Et 1. BuLi, 2 moles 2. CH3CH,Br Ph

A: Organic reaction:

Q: Cl2 H20 ÇN „NH2

A:

Q: Show the product from the following reaction, and draw the reaction mechanism. CO₂H Br₂ NaHCO3, H₂O

A: The mechanism and the final product are given below,here NaHCO3 act as a base

Q: Question attached

A: In an organic reaction, a nucleophile attacks an electrophile.

Q: 1. Hg(OAc)2, H20 SoCl2 NaOH t-butoxide Jones PCC 2. NaBH4 2. H,O2, OH" .CI HO,

A: Given reactant is primary alcohol.

Q: ö: Br: H,0 heat ОН DH

A:

Q: 1) NaOEt + OCH3 OCH3 2) H300 МЕСНANISM

A: All details explanation in Handwritten solution.

Q: 4. Propose a mechanism for the reaction below. ( HS SH cat. H

A: Reaction-       In analogy for the formation of acetals from alcohols and acid, treatment of…

Q: 1) NaOH 2) H30° MECHANISM

A:

Q: OH OH a) CH3 b) c) Br

A:

Q: Propose a mechanism for the following reaction. -NH2 -NH-

A: To solve this problem we have to write the mechanism of the given reaction .

Q: 1. 1eq. Eto /E£OH OEt 2. H30® Dieckman cyclization product ОН Anhydride NH2 1ед. 1eq NaOH O=

A: the detailed mechanism the structure of reactant or product will show below in attach image.

Q: Kz Crz Oz> H2 SO4

A:

Q: 4

A: This is an acid base reaction followed by further Alkylation .

Q: What major product (from Figure #3) results from the following two- step reaction sequence (from…

A:

Q: CH3-Br Ag,0 C5H13N N(CH3)3 H20 (heat) (еxcess)

A: Interpretation - To write the reactant in the following reaction sequence which is given as above in…

Q: What are the best reagents to accomplish this transformation? ? Br NaCE CH, followed by H2 and Pt…

A: A chemical reaction is symbolic representation of the conversion of substances to new substances.In…

Q: Propose a mechanism for the following reaction:

A: Please find below the reaction mechanism

Q: 3. Show a mechanism for the following reaction. 8-x-8 OH NO₂

A: Answer : General Reactions :     The 2-chloro-5-methylphenol and 3 fluoro-6-nitroanisole to formed…

Q: CH3 o-nitrotoluene CH3 NH, CI NO2 CH3 o-toluidine NH3*,CI CH3 CI 2-chloro-N-o-tolilpropanami NH,HCO,…

A: The solution is given below:

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.