Please redraw the substrate to begin your answer, Please illustrate all intermediate species, and include lone pairs, formal charges, and (perfect) curved arrows in your mechanism. Illustrate and name your product(s) (use dash/wedge notation as appropriate). H-Br HÖ Hints: To start, ask yourself whether HBr is an acid or a base. Please don't make stuff up (4 pos steps, 3 possible arrows, that's it).

Q: A carbamate can be prepared by treating an isocyanate with an alcohol, as shown here. This type of…

A: Carbamate- Carbamate is polyurathane polymer. Carbamate is used in synthesis of urea. Carbamate is…

Q: Br H,0 The final major organic product is|alkene or a halo-cycloalkane or an alcohol or ether:…

A: The given alkyl bromide is a tertiary alkyl halide. Tertiary alkyl bromide reacts with the iodide…

Q: Draw and specify the complete reaction mechanism to determine the product from the reaction and…

A: (R)-3-chloro-2,3-dimethylpentane is a tertiary halide and it involves SN1 reaction with…

Q: MeOH 7 products

A: This is an example of SN1/E1 reaction as the nucleophile is weak, solvent is polar-protic and…

Q: CH3 CH3COCI/ AICI3 H₂C. CH3

A: Friedel–Crafts Acylation  Involves formation of a complex between the Lewis acid and the chlorine…

Q: 3. Use curly arrows to show the mechanism for the following transformation. Show the conformation…

A: The reaction involves the E2-elimination in which the eliminating groups are opposite to each other.…

Q: Methyl amine reacts with nitric acid. You should be able to predict the products of this reaction.

A: Nitrous acid (HNO2HNO2 or HONOHONO) reacts with aliphatic amines in a fashion that provides a useful…

Q: 6) You have decided to repeat the reaction from Question 5 using a slightly different alkene…

A: This question belong to reaction mechanism of organic compounds. Mechanism takes place via stability…

Q: ai-o-ara-ata コー +|— – CI ,CI CI

A: This question is of basic organic chemistry Reaction mechanism.

Q: НО. H3O+

A: Product of following reaction can be made by applying appropriate reaction mechanism.

Q: ) Provide a reaction mechanism for the following reactions and name the major product for each. HBr…

A: SOLUTION: Step 1: 2-methyl-2-butene reacts with HBr to form 2-Bromo-2-methyl butane as a major…

Q: oft انسار Eto Nat

A: Michael addition reaction: alpha , beta unsaturated esters undergo addition reaction when treated…

Q: Write a mechanism for this reaction: Br Br2 H₂O + OH Br он

A: Alkene reacts with bromine and water to form beta bromo alcohol. The reaction follows the…

Q: Draw the reaction mechanism and the major organic product(s). HI C- CI NH + + CH₂OH Br methanol…

A:

Q: Write the systematic (IUPAC) name for each of the following organic molecules: structure CH3 OH OH…

A:

Q: Consider the reaction - predict the most likely PATH (singular) based on the reactants provided, and…

A: Nucleophilic substitution reactions are reactions in which a nucleophile replaces a leaving group.…

Q: Predict the products of this organic reaction: || CH3—C−NH—CH, + H₂O + HCI A No Reaction ?…

A: An arrow always depicts from a region of high electron density to low electron density ; that is…

Q: Draw the PRODUCTS of the reaction and draw the COMPLETE MECHANISM of the reaction.

A:

Q: OH 1) NaH 2) 3) Н-0

A:

Q: 7) Propose a mechanism for the formation of these products 6.0 Br CH₂OH +HBr

A: Given is organic reaction. The given reaction is nucleophilic substitution reaction. There are two…

Q: en deciding between 1,2-addition, 1,4-addition and the major reaction pathway, there's ually an…

A:

Q: Please solve this mechanism.

A: Step 1: Information: As we know that when carbonyl compound having Alpha hydrogen reacted with…

Q: 1) CH,SH 2) Н, о*

A:

Q: For each of the reaction below, draw the curved arrows and lone pairs of electrons to show the…

A: While drawing electron push mechanism, we begin the arrow from the atom that donates the electron…

Q: Give a reasonable mechanism for this reaction. Explain why it is exothermic. Н+ Дон H2O

A: Organic reactions are those in which organic reactant react to form organic products. In the given…

Q: Br Br Nal, acetone "H. CH3 H"

A: This reaction is an elimination reaction. It is known as dehydrohalogenation reaction which results…

Q: The conversion of (CH3)3CI to (CH3)2C=CH2 can occur by either a onestepor a two-step mechanism, as…

A: The mechanism of reaction (2) follows E1 elimination:

Q: N-R - NaOH(aq), A RNH₂

A: Hydrolysis is a chemical reaction that involves the breaking of a chemical bond in a molecule with…

Q: Consider the attached SN2 reaction. Question: What happens to the reaction rate in each of the…

A: SN2 is biomolecular nucleophilic substitution reaction. The reaction takes place in single step.…

Q: Consider the reaction below. a) Predict the reaction mechanism that is likely to operate between…

A: The given reaction is an example SN1 reaction stands for substitution nucleophilic unimolecular. The…

Q: ОН 1/2 1₂ + 1/3 Px + 1/3 P(OH)3

A: This reaction is the preparation of alkyl iodides from alcohols using phosphrous.This reaction…

Q: H* 2. H2O

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

Q: raw out the mechanism for each alkene product. Provide a description of the mechanism of each alkene…

A: Alkenes are synthesized from the dehydration of alcohol. This dehydration is acid catalyzed reaction…

Q: Propose a mechanism for this example of chloromethylation

A: The given reaction is,

Q: For the given molecule, highlight any nucleophilic sites in red and any electrophilic sites in blue.…

A: "Nucleophilic sites" are sites in a molecule that have high electron density and are easily…

Q: HO, OH

A: The answer is given as follows

Q: MeO CH;CH,NH2 CH,OH + O=

A: Given reaction,

Q: Draw the structures of all the possible products that can be obtained from the dehydration of…

A: Alcohol is an organic compound that has OH functional groups.They are reactive due to the presence…

Q: Which statement is true concerning the two carbocations formed by the protonation (attachment of an…

A: In the given problem we need to find the correct answer,

Q: (k) O || Ph—C—NHPh+CH,CH,—C—CI, AlCh

A: In first step acyl cation is formed, in second step amide attack to acyl cation to forms product

Q: Base catalysts speed up the nucleophilic reactions of carbonyl compounds. How?

A: given nucleophilic reactions of carbonyl compounds in base catalysts

Q: Draw a multi-step mechanism for this reaction and predict the structure of the organic product.…

A:

Q: X 2H₂O

A: A nucleophilic substitution reaction is a reaction in which a nucleophile replaces the leaving…

Q: Draw the mechanism and product for each of the reactions in Problem 18.45 when they are catalyzed by…

A: (a) The mechanism of the first compound catalyzed by a base is given below :

Q: BH

A:

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.