85. a. Propose a mechanism for the following reaction: CH30 Br + Br

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: Draw the product. Select Draw Rings More Erase H HgSO4, H20 H2SO4 -H

A: This reaction is example of hydration of alkyne .

Q: 1. Consider the following reaction: Br2 Br hv a) Draw a detailed mechanism for the initiation phase…

A: Initiation:- The reaction is initiated by the homolysis of Bromine molecule in presence of Light or…

Q: dentify the missing substrate. Hint: the initial step is a Claisen condensation. 1) LDA 2) HO 3)H0,…

A: Answer - The correct option is (B) Claisen condensation - The Claisen condensation is a…

Q: 2. Show the B-cleavage mechanism and product for following reaction -R R'

A: The given problem deals with β - cleavage reactions which are generally initiated in the presence of…

Q: Fill in the missing reagent(s) that would transform the starting material to the final product. (5…

A: Given:

Q: A OH он а. b. CH,OH с. d. CH2OH

A: A multiple choice question based on dehydration reaction, which is to be accomplished.

Q: D Fill in the reagents to complete the Synthetic and draw the final product EŁOH 30, 2. 3.

A: These reactions are studied in the enolate chemistry, Firstly base will abstract the proton to…

Q: 28. Which reagents would you use to accomplish the following transfomation?

A: Note: Since you have posted a question with multiple subparts, we will solve the first three…

Q: Draw the product of attached coupling reaction.

A: Given reaction,

Q: Draw a plausible mechanism for the [2,3] sigmatropic rearrangement shown below. (DBU is a base; Bn -…

A:

Q: 34. Select the best synthetic sequence to accomplish the transformation shown. Br A. 1. NaOEt; 2.…

A:

Q: Chemistry Help woth this three retrosynthesis. thank you Provide a retrosynthesis and a forward…

A: TM 1 : Epoxide opened with 1-napthol. TM 2 : see below. TM 3 : Ethyl benzoate is subjected to Fridel…

Q: Propose a mechanism. Br2, H20 H2C=CHCH2CH2CH2OH -CH2B.

A: Bromine reacts with alkene to form the bromonium ion. Since internal nucleophile (-OH) is present,…

Q: synthetic route + 0 |||

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Q: 1. Show the mechanism using curly arrows for the transformation of benzoic acid to benzoyl chloride…

A: Hey, since there are multiple questions posted, we will answer first question. If you want any…

Q: Circle the reducing sugars. OH OH но O но но но но HO но но он но OH HO но но OH OH но

A:

Q: Show a mechanism for how the product is formed. Your mechanism must use curved arrows to represent…

A: Given : organic reaction.  Here elimination is occuring, since weak base H2O is given, E1 reaction…

Q: Please provide 3 possible mechanisms for bromination of trans-cinnamic acid and pyridinium…

A: trans-cinnamic acid reacts with bromine to form 2,3-dibromo-3-phenylpropanoic  acid.

Q: F;C. HCI ZI

A: IMPORTANT POINTS: In this type of question where precursor is asked ,here hypothetical hit and…

Q: Propose a mechanism for the synthesis of the Vilsmaier-Haack reagent (Figure 6.11 – Bruckner). - `N'…

A:

Q: 5. Predict the product of the reaction sequence OEt NaOEV/HOEt Br(CH₂),Br 1. Br₂/ACOH 2. pyridine…

A:

Q: 1. Show the organic product formed when pentanal is heated with sodium methoxide in methanol as…

A:

Q: What is the following E2 mechanism? I tried using the wedge hydrogen on the chiral center with the…

A: t-butoxide can be used to form the “less substituted” alkenes in elimination reactions (the E2,…

Q: 20. Draw the full acetal formation scheme on your paper, and then draw in the curved arrows for each…

A: Acetals are geminal-diether derivatives of aldehydes, formed by reaction with excess amount of an…

Q: Propose a mechanism for attached reaction:

A: In this reaction, 'O' gets protonated to alcohol followed by the delocalization and the attack of…

Q: ) ezs Memyes 2) Hb O excess

A:

Q: 8. Design a synthesis of the target molecule from the starting material shown. ОН "ОН

A: The given tertiary butyl alcohol reacts with conc. Sulfuric acid and gives 2-methylpropane.  It…

Q: 24. Propose an efficient synthesis for each of the following transforma Br (a)

A: The question is based on the concept of organic reactions. We have to convert the reactant into…

Q: CH3 + НаС — сн н

A: We have to predict the mechanism for formation of given product via Michael addition.

Q: Add curved arrows to the structures shown below in order to complete the mechanism. OCH3 OCH3 НА OH…

A:

Q: What is the name of this structure.need answer fast i'll rate up

A: We are given a structure; Assuming the blue and red balls in the structure to be carbon as well…

Q: using thê ânswersS shown below. H3C-Br Br Br Br A В C 2) Which electrophile would you predict to…

A: Applying concept of SN1  and SN2 mechanism.

Q: Can someone show the fragmentations of 4- tert-butylphenol that would make 107m/z? Thank you. ОН CH3…

A: Following are the possible fragmentations of the given compound

Q: Show the Reaction of ROH with SOCl2 + Pyridine—An SN2 Mechanism ?

A:

Q: Propose a synthesis for each of the Target Molecules below. You may use any reagents you wish, but…

A:

Q: 25) Draw the Structures and mechanism for the Major produst + C Ho Na OCHE CH3OH. CHO

A: The two given reactions are best example of condensation reaction followed by removal of water with…

Q: 34. Propose a mechanism for the following reaction: H + H20 CH, CH2CH2CH2 он

A: In this question, we will draw the mechanism steps for the formation of cyclic ether from the given…

Q: Draw the structure of vanillin below. List each substitute my group name and write what type of…

A: Benzene is the simplest aromatic compound which show electrophilic substitution reactions mainly.…

Q: Draw a mechanism that satisfies the transformation below. OH Cl2 Ph H20 Ph

A: When alkene reacts with Cl2 to form cyclo chloronium ion as an intermediate in this reaction, which…

Q: Design a synthesis for the target molecule from the indicated starting material.

A: Given, Reactant = Ethyl benzene  Product = 3-Phenylpropanenitrile  Conversion = ?

Q: CI Br. NO2

A: Answer:- This question is answered by using the simple concept of chemical reactions of benzene…

Q: 15. Provide a curved arrow mechanism for the transformation below. OCH, Br2 + enantiomer Br CH,OH…

A: The correct answer is given below

Q: Provide the major product in each box for the multistep synthesis below. Mg0 Br Et,0 2. aq NH CI 55…

A: Alkyl magnesium halide is known as a Grignard reagent. The general formula of the Grignard reagent…

Q: HgCl2, CaCO3, H20 H H. HS SH S +

A: In this reaction, Hg2+ has high affinity and sulfur is an electron donating group because of lone…

Q: Provide the major product in each box for the multistep synthesis below. Mg0 1. H2SO4 Br Et20 2. aq…

A: The reactions given is,

Q: NV) Predict the products. cenade eurite 1. Mechanism ci mechandsome NH2NH2 Cao консаг

A: Aldehydes and ketones when heated with hydrazine and KOH give alkanes. This reduction is known as…

Q: Br Br2 anti or syn addition of Br2? CH3 Br 1. ВНз anti or syn addition of H20? CH3 Mark or…

A: Syn addition= addition of groups from same side Anti addition =addition of groups from opposite side

Q: Which is more effective 70% Ethyl Alcohol or 40% Isopropyl Alcohol? Why?

A: Ethyl alcohol and Isopropyl alcohol are the types of alcohols that are used in the making of hand…

Q: Q2. For the reactions below, draw out the reactions as shown and answer the following questions for…

A: This reaction example of elimination reaction.

Micelles and Biological Membrane

Micelles are the type of lipid molecules that organize themselves in spherical shape in aqueous solutions. The production of the micelle is a reply to the amphipathic behavior of fatty acids. It means that they consist of both hydrophobic regions and hydrophilic regions. In micelles, polar head groups (hydrophilic groups) produce an outer layer associated with water whereas nonpolar tails (hydrophobic groups) are organized in the interior.