Q: Which is the least stable carbocation?
A: In order to determine the stability of carbocation we have to check following factors sequencly 1)…
Q: How To Assign the Prefixes E and Z to an Alkene ? discuss by steps ?
A: E-Z designators are used as like cis-trans terminology for non-similar groups attached alkenes.
Q: 2) Using one of the MO diagrams your developed in question 1, briefly explain the origins of the…
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Q: From trans-1-chloro-2-isopropylcyclohexane, only 3-isopropylcyclohexene, the less substituted…
A: SOLUTION: Step 1: Treatment of trans-1-chloro-2-isopropyl cyclohexane with sodium methoxide in…
Q: Which of the following concepts explains why a tertiary carbocation is more stable than a primary…
A: We have to say why a tertiary carbocation is more stable than a primary carbocation?
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: Illsutrate the Energy diagram for carbocation formation in two different SN1 reactions ?
A: SN1 reaction or Unimolecular nucleophilic substitution reaction is a type of nucleophilic…
Q: Which of the following carbocations is(are) likely to rearrange? a. I b. II c. III d. II and III…
A: Rearrangement occurs due to increase the stablity of carbocation.
Q: Define Carbocation Stability?
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Q: IUPAC NAMING and Indicate the stereochemistry if E or Z. Write the complete solution
A: For IUPAC naming following steps are required- First of all identify the longest carbon chain…
Q: Pentene is a most elusive molecule that has never been isolated before. However, the pentalene…
A: The stability of the hydrocarbon that has an unsaturated system of π bonds and its aromatic nature…
Q: (b) Discuss about the stability factors of the reaction intermediates, which involved in a name…
A: The answer is as follows:
Q: а) b)| Br
A: Applying concept of IUPAC nomenclature of organic molecules.
Q: In the alkene below, why is HB more easily abstracted by a halogen atom than HẠ ? НА HB A.…
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Q: Rank the following radicals in order of decreasing stability. most stable least stable (сны,снінсн,…
A: The stability of carbon free radicals can be determined by considering the number of hypercojugative…
Q: Arrange carbocation in order of increasing stability
A: More the hyperconjugation, more is the stability of the carbocation.
Q: Conceptual: Rank the following alkenes in decreasing order of stability. b
A: The relative stability of the alkenes can be understood by the presence of hyperconjugative H atoms.…
Q: a. How many s bond orbitals are available for overlap with the vacant p orbital in 1. the isobutyl…
A: An orbital is a 3D description of the location of an electron around an atom. s, p, d, f and so on…
Q: Rank the carbocations in the Figure below in order of decreasing stability. ["~" = approximately…
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Q: For the following pair of carbocations (A and B), select the one that is more stable and explain…
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Q: Rank the attached radicals in order of increasing stability
A: Free radicals refer to the type of reactive intermediate in which a homolytic cleavage of bond takes…
Q: Carbocations rearrange with some ease. An example of this is shown below. Indicate, with the…
A: Rearrangement of carbocations takes place to produce more stable carbocations.
Q: Rank the stability of the following alkenes from least to most stable. а. b. с. (А) а, b, с (B) b,…
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Q: b. С. + + + a.
A: The reactive intermediate species in which carbon atom forms only three bonds and contains a…
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: Question 7 of 12 Submit Identify this mechanistic step in a radical halogenation reaction. CI- CI UV…
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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: Explain the Stability of Allylic Carbocations ?
A: Carbocations are positively charged, sp2 hybridized trigonal planer structures. They are electron…
Q: Give evidence, through specific examples (research on the internet), to support the carbocation…
A: Markownikoff’s rule- Negative ion of reagent gets added to carbon of alkene which is more…
Q: Place the following cyclic compounds in order from highest to lowest stability. For the lower…
A: cyclopropane and cyclobutane are less stable than cyclohexane, because the smaller rings are more…
Q: Explain why CH3CH2CH2CH2Cl reacts with 0.01M NaCN in Ethanol (C2H5OH) to yield primarily…
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Q: %3D
A: Resonance is defined as delocalization of pie electron . Electrons are flowing from high density to…
Q: Draw geometrically clear picture of the most stable enol form of the compound shown below, and point…
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Q: (a) How the thermodynamic parameters explain the stability of an organometallic compound? Explain…
A: Ligands play an important role in stabilizing transition metal complexes. Therefore, the stability…
Q: (4B) Carbocation Stability: Rank the following carbocations in order of stability and briefly…
A: Carbocation is species in which carbon bears positive charge.
Q: The first alkene which requires the position of the double bond to be indicated is?
A: Alkene contains a carbon-carbon double bond and for this minimum two carbon atoms are required.
Q: Why the relative reactivity of SN2 is tertiary<secondary<primary<allyl, phenyl ? (explanation)
A: In this question, we will discuss on relative reactivity of SN2 you can see the explanation below.…
Q: Using the resonance theory which carbocations is more stable ? And why ?
A: When a single Lewis structure fails to explain all the properties of a molecules resonance comes…
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: For each of the alkyl bromides, do think it is likely to form the you substitution or elimination…
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Q: Write with additional resonance contributing structure for each carbocation and state which of the…
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Q: Which of the following statements are true of an SN2 reaction. follow a first order rate law a b…
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Q: Arrange the compounds in increasing order according to its stability of carbocation
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Q: Rank the followings carbocations in terms of increasing stability (least to most)
A: Stability of carbo cation depends upon the type of structure of carbocation , primary are least…
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: 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…
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- How To Assign the Prefixes E and Z to an Alkene ? discuss by steps ?The following is generic depiction of a reaction using the curve arrow formalism. -D Which of these statements is not correct for this reaction? Electrons move from C to B. Electrons move from B to A. O In the products, a bond forms between C and B. O In the products, A would have a positive charge.Determining the Relative Energy of Resonance Structures and the Hybrid Draw a second resonance structure for carbocation A, as well as the hybrid of both resonance structures. Then use Rules [1]–[3] to rank the relative stability of both resonance structures and the hybrid.
- Define Carbocation Stability?Question (Organic Chemistry) Consider molecules A–D. Does the arrow pushing in each structure leadto an acceptable resonance form? If so, explain why it is acceptable or unacceptable? What are the rules and logic? If so, draw it and carefully explain your answer and provide explanations for why each structure leds to an acceptable or unacceptable resonance form. Why is the arrow pushing acceptable or unacceptable in each individual case? Explain you answer with many details, logic, and in a step-by-step fashion.Question (Organic Chemistry) Consider molecules A–B. Does the arrow pushing in each structure leadto an acceptable resonance form? If so, explain why it is acceptable or unacceptable? What are the rules and logic? If so, draw it and carefully explain your answer and provide explanations for why each structure leds to an acceptable or unacceptable resonance form. Why is the arrow pushing acceptable or unacceptable in each individual case? Explain you answer with many details, logic, and in a step-by-step fashion.
- Question (Organic Chemistry) Consider molecules A–B. Does the arrow pushing in each structure leadto an acceptable resonance form? If so, explain why it is acceptable or unacceptable? What are the rules and logic? If so, draw it and carefully explain your answer and provide explanations for why each structure leds to an acceptable or unacceptable resonance form. Why is the arrow pushing acceptable or unacceptable in each individual case? Explain you answer with many details, logic, and in a step-by-step fashion. Please explain your rationale or logic. The answers provided on Bartleby lack a clear rationale and explanation of why the octet rule matters or why electron rich and electron deficient sites are important to this drawings.Please give a clear handwritten answer of both sub parts reactions what will be major product...! ( give step by step explanation)
- If the elimination reaction can result in the formation of two different alkenes which one with predominate in the product?Please give a explaination for each moleculeOChem help with the following reaction schemes (see attached image) Please provide the bond line structures for the products obtained in the following reaction schemes... Notice in question #1 that A, B, and C are actually shown as C, B, and finally A in the actual reaction scheme so C correlates with PCC, and so on Question #2 is in order.