show all steps. and mechanismplease follow the requirments i mentioned. 4- Propose a synthetic pathway for each of the following compound Show all steps.Starting from Benzene ringNH2

The given compound has an alkyl group substituted at the para position. The first step in the…

Answered: 4- Propose a synthetic pathway for each…

Science

Chemistry

4- Propose a synthetic pathway for each of the following compound Show all steps. Starting from Benzene ring NH2

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter26: Aldol And Claisen Reactions

Section: Chapter Questions

Problem 26E

See similar textbooks

Related questions

Q: Mechanism 1. Propose a mechanism that accounts for the transformation below. TSOH, EIOH EtO…

A: This reaction proceeds through SN2 mechanism.

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

Q: OEt EtO OEt

Q: H2SO4 CH;CH;CH=CH, + CH;OH CH;CH;CHCH; ÓCH3

A: In the reaction of alkene with alcohol in presence of acid, first the alkene takes proton from the…

Q: List the best reagents to carry out the following conversions: (a) OH HO,

A: As you have posted multiple independent questions, we will solve the first question for you. To get…

Q: 5. Complete the following reaction and propose a mechanism to justify your ane 1. O3 ? 2. Reductive…

A: Alkene on ozonolysis gives carbonyl group.

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: Will the following bases favor an E1 or E2 mechanism? Sort them into the appropriate boxes below.…

A: Strong base favour E-2 reaction and weak base favour E-1 reaction.

Q: OH Propose a mechanism for the reaction shown here. Note that the reaction does not take place…

A: The mechanism for the given reaction is to be drawn. The reaction is, This is the epoxide ring…

Q: ix. In STEPS 9-10, a hydroxide ion causes the anhydride to break down and cleave into two products.…

Q: 2. Soclz 3. cexcess) TSOH (cat),

Q: 4-) Complete the following diazocoupling reaction.

A: Aniline derivatives upon treated with nitrosyl cation to give diazonium salt , it is like…

Q: 6. A synthesis of a molecule being explored as an antidepressant drug (J. Org. Chem 2012) utilized…

A: AlCl3---> It is a lewis acid. it accepts the electron. CH2=CH2 (Ethene): It acts as a nucleophile…

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

A: We have to propose a synthetic pathway for molecule X to molecule Y using the reagents boxed below…

Q: 1. B. Supply the missing arrows to complete the reaction mechanisms below. For each of the…

A: Electrophile are electron acceptor while nucleophile are electron donor.

Q: OH HO Br HO

A: The question is based on the concept of chemical conversions. we have been given reactant and…

Q: :ÇI: 3. Write a complete, detailed mechanism for the reaction to the right. Be sure to clearly…

A: Here i have explained the mechanism of the reaction

Q: I need help with the mechanisms on these two reactions please :) NaOH A b. 1. Draw a complete arrow…

A: b.)

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

Q: 2. Draw the appropriate mechanism for the following reaction. Me Me H*, MeOH Me OMe Me OMe

Q: Show a reasonable mechanism for how the following reaction comes about OH NaONO H30* H2N

Q: 3. Show the reaction mechanism for the following multistep transformations. Show all reagents and…

A: Alcohol is converted to bromide by PBr3 and then it is converted to Grignard reagent and that reacts…

Q: OMe cm Clz mCP BA MeO `OH

A: Given reaction is example of Baeyer-Villiger oxidation. The Baeyer–Villiger oxidation is an organic…

Q: HO Provide a mechanism for the transformation below. HO H,O/ CH;OH :0:

A: A reaction mechanism is the order of basic steps by which a chemical reaction occurs. A reaction…

Q: 3. Show the step(s) necessary to carry out this transformation: cyclohexanone →…

A: When ketone react with primary amine then it forms immine. It is formed under acidic conditions.…

Q: 4. Propose a mechanism for the SUBSTITUTION reaction below: HINT AICI, is an ELECTROPHILE. H3C ÇH3…

A: The given reaction is a Friedel - Crafts alkylation reaction. In this reaction alkylation of…

Q: 2. Assume all reactions add the reagent once. Will the following reactions produce the major product…

A: Electrophilic addition reaction will favour at that position where electron density is high . Note:…

Q: Select the correct reagents to carry out the following multi-step synthesis. CH3 CH2-Br CH,-OH CHO…

A: 1. Fridel craft alkylation is electrophilic aromatic substitution reaction in which benzene acts as…

Q: Show a possible mechanism for the following reaction CN CO,Me CN.

Q: HO 1. LIAIH4 2. H20 HO HO HO.

A: Mechanism

Q: ~NBU2 HO NaOH H. CI ELOH

A: The first step of the reaction involves the acid-base reaction. The NaOH being a strong base will…

Q: 6. A synthesis of a molecule being explored as an antidepressant drug (J. Org. Chem 2012) utilized…

Q: Question attached

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

Q: Predict the major product of the given reaction and then draw a reasonable mechanism for the product…

A: Given, Draw the mechanism = ?

Q: .CH 3 CM 3

Q: H. HEAT ENDO PRODULT Exo FRODUCT XO

A: Both are Dieles Alder reactions and give Dieles Alder Product via [4+2]π cycloaddion reaction. You…

Q: Can someone please show me a step by step mechanism of this reaction?

A: The given reaction is

Q: C. Show the product formed in each step of this multi-step synthesis. Br2, H3O+ KOtBu immmmmm NaOH,…

A: The answer is as follows:

Q: Он. OH N OH H. - NH2 + H H. OH HO, OH OH Охalic Acid OH

Q: For each of the following reactions, determine which ELIMINATION mechanism (E1 or E2) will occur.…

A: Elimination reaction: E1 elimination reaction with major product

Q: *NH H*

A: Reactants are secondary amine and ketone, medium of reaction is acidic medium.

Q: Ph Na Oet Eto OEt

Q: 5. Provide an efficient synthesis for the following transformation. Synthesis with the fewest steps,…

A: When a molecule has O=C(R1)-C=C-R2 structure, it is termed as the alpha beta-unsaturated carbonyl…

Q: N H .N. NaNH2 CI CI

Q: Match each reaction sequence to a product below. Assume any necessary workup. Answers may be…

Q: 3. Provide the major product of the following reactions. Show the complete mechanism for products A,…

A: Above reactions are the nucleophilic substitution and elimination reactionsl of the alkene.

Q: HBY Cexcess) -> 4.

Q: Draw the product of the reaction. 2 equiv. HO, H*

A: A question based on organic reaction, which is to be accomplished.

Q: benzaldehyde 9 H ethyl formate -OCH₂CH3 1. pyrolidine O 2. 3. H₂O* 8 10 ya ii + excess benzaldehyde…

A: Since you have posted a question with multiple sub-parts, we will solve the first three subparts for…

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…

Concept explainers

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.

Question

show all steps. and mechanism please follow the requirments i mentioned.

4- Propose a synthetic pathway for each of the following compound Show all steps.
Starting from Benzene ring
NH2

Expert Solution

This question has been solved!

Explore an expertly crafted, step-by-step solution for a thorough understanding of key concepts.

SEE SOLUTION Check out a sample Q&A here

Step 1

VIEW

Step 2

VIEW

Step by step

Solved in 2 steps with 1 images

SEE SOLUTION Check out a sample Q&A here

Knowledge Booster

Learn more about

Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.

Similar questions

Cs Scanned with CamScanner 2. Show two reaction schemes to synthesize the following compounds. Pick one reaction scheme and draw the step-by-step reaction mechanism. а. HO-
Draw the major organic product of the reaction shown below. OH H2SO4
Do the reactions below proceed in good yield from left to right as shown? Please fill in Yes or No
For the reaction sequence below, provide the correct reagents, intermediate or final product. Br You? Na enant.
Draw the major organic product of the following reaction sequence. 1) RCO₂H 2) NaSMe 3) H₂O* ? || \ ²+1 +1 +1 +1 - 02 محمد L I UZ O a F 2-29 Br
T 3. The first product made in an acid catalyzed hydration reaction of an alkyne is an unstable functional group called an enol. Enols quickly tautomerize to a carbonyl (either ketone or aldehyde). Starting with the enol, sulfuric acid, and water, draw the complete, detailed mechanism for this acidic tautomerization reaction below. Q Search 6 & 7 Alkyne HgSO4 H₂SO4 H₂O 8 fg OH Enol lyi 9 f10 Ketone O f12 +
2. Draw a detailed mechanism for the following reactions. You do not need to draw arrow steps for the hydrogenation reaction. Ph 1. NaOH 2. CH31 3. H₂ Pd/C 4. H30* HBr en Ph^ Br
ts) Circle the correct reactant to make the following epoxide. H OH Ph Ph OH Ph H Ph Br OH OH Ph Ph "OH P HE
1. Reactions: Draw the major organic product for the following reactions. When required, indicate the mechanism by which each reaction proceeds in the small box provided below the reaction arrow. a) Br EtOH, A EtOH b) d) e) OH TsCl pyridine KO'Bu HO'Bu H H Br NAOMe HOME H₁ NaCN DMF LDA NaOH Et₂O H₂O H₂O, A 음음 Br
Use your general knowledge of alkene chemistry to suggest a mechanism for the following reaction.
Draw the alkyl bromide for reaction 2. Select Draw Rings More Erase | 7 | | H Br Reagents Carboxylic Acid Product 1. Diethyl malonate, NaOC2H5, C2H5OH 2. NaOH, H2O 3. H3O*, heat ОН Draw the alkyl bromide for reaction 3.
3. Why do the following two reactions not proceed under basic conditions? Draw the mechanism of each up until the point of failure under basic conditions. HO * OH 4 basic conditions HN Ph * basic conditions