OH N 3HCI NH₂ 12 (not isolated) 11 (not isolated) HN (pyronaridine) ♡° 75 °C, 16 h 95% (3 steps) OH

Q: Detailed reaction mechanism:

A: The explanation is given below-

Q: c) Hg(OAc)2 H₂SO4, H₂O I I

A:

Q: Explain Reimer tiemenn reaction with mechanism

A: The Reimer-Tiemann reaction is a reaction in which phenol reacts with chloroform in the presence of…

Q: Determine the mechanism of nucleophilic substitution for attached reaction anddraw the products,…

A: INTRODUCTION: SN1 reaction is a two step reaction in which first carbocation is formed that acts as…

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

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Q: i) NOCI/ py HO ihu CO,Me

A: The first reaction is Barton reaction. Barton reaction is a photochemical reaction that involves the…

Q: Consider the reaction scheme shown below. HCI [1] HO. (a) Provide a detailed mechanism for reaction…

A: This reaction will occur via 3 step. In first step protonation then Water molecule eliminate to…

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: H2, Pd/C HSPH base (cat)

A:

Q: OH N NO₂ 11 (not isolated) 1% Pd/C (2 mol % Pd) H₂ balloon, HCI (3 equiv) 2 wt% TPGS-750-M/H₂O 75…

A: Mechanism of the reaction

Q: REACTION #3 (1 elementary step): Name of Elementary Step:_ H Но + H. H. H REACTION #4 (1 elementary…

A: Following are the curved mechanism of the given organic reactions.

Q: (b) How can be prepared from OEt CO,Et and at EtO OEt EtO2C 95 °C ? Provide the mechanism.

A:

Q: NO2 HBF4 Br, FeBra H2, Ni NANO2, H0*

A: We have to predict the major product from the given reagents.

Q: When ethylbenzene reacts with bromine in a free radical halogenation, a small amount of product that…

A:

Q: which

A: Nucleophilic substitution reaction in which an nucleophile substitute any group from reactant.

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

A:

Q: ОН

A: These reactions are generally proceeds in a heating or light conditions.  Here we are given with…

Q: H* 2. H2O

A: Alkene mainly gives electrophilic addition reaction in which an electrophile attacks on electron…

Q: `N مونه CI (excess)

A: Acylation of amines: Primary and secondary amines containing replaceable hydrogen atoms react with…

Q: Draw the complete reaction mechanism of the following reaction. Explain each step

A: The reaction given is,

Q: но ногом 0 Н. ен Н. за у (osnx7) Н -он

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Q: МСРВА

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Q: waF

A:

Q: Give the detailed mechanism for the following nitration reaction. Show the contributing resonance…

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

Q: (с) HCI (d) HCI

A:

Q: Which of the following reactions willactually yield the indicated product?

A: The given following reaction is actually yield the indicated product can be identified

Q: ga h. i. ZH N N S + C6H5N=N CH3 Br 1. NH₂ 2. CH3CH₂CH₂Br 1. Mg/Et₂O 2. CO₂ 3. HCI

A: Given reactions are shown below.We have to draw the product of those reactions with the mechanism.

Q: Which of the following reactions occurs more rapidly?

A: The reaction which occur most rapidly is the reaction in option B as Epoxide is getting formed in…

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: R-O-O-R

A: This is Free radical decarbonylation. 1st product is without radical rearrangement via less stable…

Q: Determine the mechanism of nucleophilic substitution of attached reactionand draw the products,…

A: Dimethylformamide or DMF is a colorless organic liquid which is miscible with water and many organic…

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

A: