OH (d) (d) 1. BH3 THF (c) HBL IH (b) 2. H2O2, H20 Seun el pnwolot ort lo orlW E (e) 1. Oaneming eub el nodo noteuoomoKo erd o ytonleoT lo aslea erl ino heminq oub a 2. Me2S ming eub al noitosoT tbele of yinemihq eub al notodoibyl mpo eri lo ylivi byrd er to yiv

Q: help please answer in text form with proper workings and explanation for each and every part and…

A: Step 1: Anti-Markovnikov's Rule:Principle: Anti-Markovnikov's rule states that in the addition of HX…

Q: Draw the major organic product of the reaction. Show the stereochemistry, if applicable. Omit…

A: Introduction: When an alkyl halide is treated with a nucleophile, it removes the halide ion. t-alkyl…

Q: The reaction shown forms two major substitution products. Draw both products and write a mechanism…

A: The compound given is tertiary alkyl halide which reacts with Methanol by Unimolecular Nucleophilic…

Q: -OH/H20 ACCI, pyridine H* /H2O

A:

Q: None

A: Step 1:This is a subsitution reaction. Br is a good leaving group. We also have a primary alkyl…

Q: REVIEW CHALLENGE: 4. Show how you can carry out the synthetic conversions indicated in an efficient…

A: The question is based on the concept of organic synthesis.We need to synthesize the product using…

Q: NaCN acetonitrile

A: Acetonitrile is an organic compound having the chemical formula CH3CN. In the above reaction…

Q: Draw all products for each of the following reactions or reaction sequences. For chiral molecules…

A:

Q: None

A: Step 1: Reagents Needed:Bromine (Br₂): Bromine will be used as the source of bromine atoms for the…

Q: What are the errors in the following answer?  Note: If the product has ortho or para substitution,…

A: In a substitution reaction, one substituent in a chemical compound is replaced by another.  When a…

Q: Write structures for the carbonyl electrophile and enolate nucleophile that react to give the aldol…

A:

Q: Can you help propose a sy

A: 1. Cyclohexane is converted in to cyclo-1,3-hexadiene :  cyclohexane upon treated with chlorine…

Q: Draw an alkyl halide that would undergo an SN2 reaction to yield this product under the conditions…

A:

Q: Please help 2d

A: Carbocation rearranges from less stable to more stable carbocation. Stability order of carbocation…

Q: Curved arrows are used to illustrate the flow of electrons. Using the provided starting and product…

A: Dehydrohalogenation by E1 mechanism takes place in the following steps:  Step 1 : Halide ion leaves…

Q: For the dehydrohalogenation (E2) reaction shown, draw the Zaitsev product(s) resulting from…

A: Find the product.

Q: First, identify the reactions taking place. Look at the reagents over the arrows. What is the first…

A: 1.  With 1st reaction, OH Group reacts with Tscl,Pyridine. It becomes OTS. Then OTS  group is good…

Q: Draw the major products of this reaction. H3C. Br,/FoBr, Create OscerSketch Answer 1 Draw the…

A: Aromatic electrophilic substitution reactions are the characteristic feature of benzene and other…

Q: A. Predict the major product of the reaction. Clearly indicate stereochemistry, if necessary. B.…

A: The given reaction is an E2 elimination. There is a specific stereoelectronic requirement for E2…

Q: draw the reagents necessary to prepare this product through two different reactions. Draw the…

A: Given is organic compound.To find out starting compound, let's perform retrosynthetic analysis of…

Q: Can the target compound at right be efficiently synthesized from the starting material at left?

A: Given is organic synthesis reaction.The given starting compound is primary alkyl bromide.The given…

Q: Consider the reaction of 2,2,4,4-tetramethylpentane with chlorine in light. The first step is…

A: During homolytic cleavage, the lone pair electron present in the sigma bond is equally distributed…

Q: Draw all products for each of the following reactions or reaction sequences. For chiral molecules…

A:

Q: Include all lone pairs and charges as appropriate. Ignore stereochemistry. Ignore byproducts. 0.01 M…

A: The E1 reaction (Elimination Unimolecular) is a type of elimination reaction in organic chemistry…

Q: For the following multistep synthesis of the target structure on right from the starting structure…

A:

Q: 6. Write a complete multi-step synthetic route for the transformation to the right. -NO2 You may use…

A: Given: To determine the multi-step synthesis of benzene into  4-nitrobromobenzene.

Q: 3.Complete the reactions below by drawing the major product or products. Indicate product…

A: In a SN2 reaction, the nucleophile attacks from the opposite side of that of the leaving group. The…

Q: heat OH

A: In the above reaction, reactant in presence of H3O+, dehydration and rearrangement takes place.

Q: For the following multistep synthesis of the target structure on right from the starting structure…

A:

Q: Can the target compound at right be efficiently synthesized from the starting material at left? Br…

A: Target molecule can be synthesized from the starting material.But not through substitution…

Q: Draw the major organic product(s) of the following reaction. 'Br + excess NH3 H₂O

A: Given is organic reaction.The given reactant is alkyl bromide.The given reagent is excess…

Q: Draw all products for each of the following reactions or reaction sequences. For chiral molecules…

A:

Q: Draw a valid and complete reaction mechanism, including all stereochemistry for the reaction shown.…

A: There are number of functional group associated with organic compounds which impart specific…

Q: Select any and all Diels-Alder endo products from this set of molecules. Choose one or more: H H H…

A: In endo product the electron withdrawing group from the dienophile is directed towards the newly…

Q: Match each alkyl halide to the appropriate descriptor. Some descriptors may be used more than once,…

A: The classification of carbon atoms is done on the basis of the number of carbon atoms attached to…

Q: raw all steps in a proposed synthetic pathway to convert the given starting material to the…

A: Alkene reacts with hydrogen bromide in the presence of hydrogen peroxide to form a alkyl halide…

Q: CA C Synthesis using a multiple RXN. A desired alkene product is shown below. A starting material is…

A: The question is based on the concept of organic synthesis.We need to synthesize the product using…

Q: 2. Show how to carry out the following transformation. ? OMe Br Show all required reagents and the…

A: At first NH2-CH2-CH(Br)-OMe is synthesized by Williamson ether synthesis from NH2-CH2-CH(Br)-O-H.…

Q: Draw both resonance structures of the most stable carbocation intermediate in the reaction shown.

A: The cation that acts as a intermediate in the reaction is known as carbocation. In carbocation,…

Q: 2. Draw the major product of the following E2 reaction. Show stereochemistry where appropriate.…

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.