Q: Why is there a difference in racemization for the two reactions even though they both include the…
A: Bromine is an excellent leaving group compared to hydroxyl group. Hence, in case of 2-bromobutane,…
Q: give the major products of each reaction
A: We have given three organic reactions. Major product : the major product of reaction is the product…
Q: a) N.
A:
Q: Give the machanism of this reaction
A:
Q: Explain why compound A is much more stable than compound B.
A:
Q: Show, in increasing order, the relative stability of the following carbocations
A: Stability of carbocation intermediate can be explained in terms of number of hyperconjugative…
Q: a. How many vinylic hydrogens does cyclopentene have? b. How many allylic hydrogens does it have?
A: a) The hydrogen which is bonded to a vinylic carbon (sp2 carbon of an alkene) is called vinylic…
Q: Consider this scheme. Why does a ring form with a single ethylene glycol on A rather than two…
A: A single ethylene glycol on A rather than two molecules of ethylene glycol to form acyclic acetals…
Q: (A) Provide the major organic product for the reaction below (B) Would the product be optically…
A: Sugar undergoes oxidation reaction in presence of HNO3 . Both aldehyde and alcohol group is oxidis
Q: Draw the product of this nydrogenation reaction. Use wedge and dash bonds to indicate…
A: Interpretation: We have to determine the product for the following given reaction.
Q: ... in water in dilute acid. ㅈ
A: Given : structure of reactant.
Q: 5. Write the stepwise mechanism for the following reaction. Show all electron flow with arrows and…
A:
Q: (b) Discuss about the stability factors of the reaction intermediates, which involved in a name…
A: The answer is as follows:
Q: 4) What happens to the stereochemistry during and SN2 reaction? Why? Provide a reaction to…
A: SN2 reaction is bimolecular nucleophilic substitution reaction. This is single step reaction that…
Q: 4. Write a complete stepwise mechanism for any TWO of the following. You need to use curved arrows…
A:
Q: Explain and give examples of the stability order of carbocations within the group and among…
A: Carbocation: Carbocation is spices that carries carbon with a +ve charge. It is of 4 types…
Q: Arrange carbocation in order of increasing stability
A: More the hyperconjugation, more is the stability of the carbocation.
Q: "green" oxidation The above reaction is one of example of environmental benign synthesis which does…
A: Green oxidation requires use of hydrogen peroxide and oxidation.
Q: Rank the carbocations in the Figure below in order of decreasing stability. ["~" = approximately…
A:
Q: For the following pair of carbocations (A and B), select the one that is more stable and explain…
A:
Q: what is the alkene that would give the product ( a or b)?and why?
A: Alkenes are the compounds that contain at least one carbon-carbon double bond. These compounds…
Q: Rank the following carbocations in order of decreasing stability, putting the most s II Multiple…
A: Stability of carbocation is as 3°>2°>1° We can see that I is a 3° Carbocation as the carbon…
Q: ,including all stereoisomers of the product.
A: This reaction is Dieles Alder reaction because it's have diene and dienophile Compound in the…
Q: Below is a schematic representation of possible reactions that Compound X can undergo. Use the…
A: Hi, since there are multiple subparts posted. we will provide you with answers for the first three…
Q: Qustion below attached .
A: Hello. Since your question has multiple sub-parts, we will solve first three sub-parts for you. If…
Q: Explain why compound A is much more stable than compound B.
A: The compare the stbaility of the two compounds above we check whether the compound is aromatic or…
Q: give the all stereoisomers with explanation for the given bleow structure ..
A:
Q: Explain why compound A will not undergo a ring-opening reaction under thermal conditions, but…
A: Ring opening reactions for A and B are given below :
Q: Rank the attached alkenes in order of increasing stability.
A: Alkene stability depends on Degree of hyper conjugation.
Q: Explain why compound A will not undergo a ring-opening reaction under thermal conditions, but…
A:
Q: Explain why compound A is much more stable than compound B.?
A: The compound A is more stable than compound B has to be explained below,
Q: use molecular orbitals to rationalize why c=o is more prone to involve in a reaction with a…
A: Here we have to rationalize the cause why C=O is more prone to involve in a nucleophilic reaction…
Q: Convert each ball-and-stick model to a skeletal structure that clearly shows the stereochemistry at…
A: Concept introduction: Decalin and its derivatives involve fusion of two six membered rings that…
Q: Provide the structure of the product(s) with stereochemisty if appropriate. If multiple products…
A: Indicate major product of Given reaction
Q: Below is a schematic representation of possible reactions that Compound X can undergo. Use the…
A:
Q: 1. Compound2 may have an electrophilicreaction because of its saturation 2. Compound1 must undergo…
A: Since double bonded and triple bonded compounds are in unsaturation condition whereas single-bonded…
Q: A)What is the IUPAC name for Compound X? B)What type of reaction (s) is/are represented by (i) and…
A: SOLUTION: Step 1: Hello. Since the question has multiple parts, the first three parts has been…
Q: How many mono chlorinated products excluding stereoisomers? I believe it is 5 but if someone can…
A: Free radicals are reactive species that contain an odd number of electrons on an atom. Example:…
Q: (a) Arrange the following compounds according to their reactivity towards electrophile. Justify your…
A: We must know that more aromatic a compound is, more stable it will be and thus less reactive. A…
Q: a. b. HBr, A Peroxide NBR, A Peroxide
A: In reaction a) Alkene is treated with HBr in presence of peroxide which follows anti markonikov's…
Q: Unlike most hydrates, the hydrate of cyclopropanone is stable and can be isolated. Explain why this…
A: The reaction for the formation of hydrates from cyclopropane can be given as:…
Q: B D Write the letters that correspond to the starting material and the product for the mechanistic…
A: In this question, you give the letters for starting material and Product ( on the right side energy…
Q: The of alka zeltzer in iced water will give a result and observation of _________. alka zetltzer…
A:
Q: The alkyl halide shown below in line-bond structure is the product of ethene hydrohalogenation.…
A: Answer - The correct option is - A , B and D Explanation - According to the question - A, B and D…
Q: (a) Discuss the aromaticity of a six membered heterocyclic compound which is weak base in nature.…
A: The solution is as follows:
Q: a) place asterisks(*) at the allylic position of compound A. b) Draw the resonance forms of the…
A:
Q: N 애 웅도
A:
Trending now
This is a popular solution!
Step by step
Solved in 2 steps with 2 images
- 1. Give the major organic product(s) of the reaction and include all the stereochemistry as appropriate. Identify any meso compounds. 2. Indicate whether a solution of the product would be optically active or no not active and provide a simple reasoning to support your choice. Need the last 2A. Provide a stepwise mechanism for the formation of nerolidyl pyrophosphate fromfarnesylpyrophosphateB. Provide a stepwise mechanism for the formation of carbocation 1 from nerolidyl pyrophosphate.Number the backbone carbons of nerolidyl pyrophosphate from 1 to 11 as shown, and include thecarbon numbering in your structure of 1C. Following from B, give an arrow-pushing mechanism to convert 1 to 2 and 2 to 3. Use thebackbone carbon numbering from 1 to indicate where carbon atoms ended up in 2 and 3D. In addition to forming epi-cedrol, carbocation 3 gives three minor byproducts: a diastereomericalcohol and two alkenes. Draw mechanisms that could give rise to these three productsWith respect to the CIP rules, assign the groups high or low priority - also what is the overall stereochemistry of the double bond?
- 1. Give the major organic product(s) of the reaction and include all the stereochemistry as appropriate. Identify any meso compounds. 2. Indicate whether a solution of the product would be optically active or no not active and provide a simple reasoning to support your choice.(−)-Hyoscyamine, an optically active drug used to treat gastrointestinal disorders, is isolated from Atropa belladonna, the deadly nightshade plant, by a basic aqueous extraction procedure. If too much base is used during isolation, optically inactive material is isolated. (a) Explain this result by drawing a stepwise mechanism. (b) Explain why littorine, an isomerisolated from the tailower plant in Australia, can be obtained optically pure regardless of the amount of base used during isolation.Grignard reagents react with oxirane (ethylene oxide) to form 1° alcohols but can be prepared in tetrahydrofuran solvent. Why is this difference in behavior observed? A. There is a better leaving group in the oxirane molecule. B. Steric hindrance in the case of tetrahydrofuran precludes reaction with the Grignard. C. It is easier to obtain tetrahydrofuran in anhydrous condition. D. Oxirane is a cyclic ether, while tetrahydrofuran is a hydrocarbon. E. The oxirane ring is the more highly strained.
- When the nitrogen-containing aromatic heterocyclic compounds 1 and 2 are treated with HCl, only 1 forms the hydrochloride salt, whereas compound 2 is unreactive. Provide an explanation for this observed reactivity.Hydrocarbon 10 and ester 12 react upon heating to give a cycloaddition product D. (i) Suggest a structure for product D and provide a curved arrow mechanism that accounts for its formation. (ii) Draw the molecular orbitals corresponding to the HOMO of 10 and the LUMO of 12 and show that these are of suitable symmetry for a concerted cycloaddition to take place. (iii) Use frontier molecular orbital theory to account for the observation that the formation of D is faster in the presence of AlCl3. please answer all thank youPhenols are less acidic than carboxylic acids, with values of pKa around 10. Phenols aredeprotonated by (and therefore soluble in) solutions of sodium hydroxide but not by solutions of sodium bicarbonate. Explain how you would use extractions to isolate the three purecompounds from a mixture of p-cresol (p-methylphenol), cyclohexanone, and benzoic acid.
- most of the additions of bromine to double bonds gave entirely antistereochemistry. Explain why the addition to phenanthrene gives a mixture of synand anti stereochemistry(a) How many Stereoisomers are possible for 9,10- dibromoexadecanoic acid?(b) Addition of bromine to palmitoleic acid primarily yields a set of enantiomers, (±) -three-9,10-dibromohexadecanoic acid. The addition of bromine is an anti-addition to the double bond (ie, it appears to occur through the intermediary of the bromonium ion). Taking into account the stereochemistry of the cis double bond of palmitoleic acid and the stereochemistry of adding bromine,Write a three-dimensional structure for (±) -three-9,10-dibromohexadecanoic acid!Although dehydrohalogenation occurs with anti periplanar geometry,some eliminations have syn periplanar geometry. Examine the startingmaterial and product of attached elimination, and state whether theelimination occurs with syn or anti periplanar geometry.