Q: it is the correct order of stability of the following radicals (more stable > less stable)?
A: Carbon forms four bonds to complete its octet. In the formation of free radical,carbon has formed…
Q: Rank the carbocation compounds below from most stable to least stable.
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Q: Which of the following rings is the most strained? cyclopropene; cyclopropane; cyclobutane;…
A: Cyclopropene is more strained among the all other rings. Usually in comparison of cycloalkanes,…
Q: Which one of the following radicals is the most stable?
A: A radical becomes highly stabilized when resonance is presence in it.
Q: 3. Compare the following three isomeric dienes: (a) Which compound will liberate the least heat upon…
A: The heat of hydrogenation is defined as the amount of energy liberated when an alkene or unsaturated…
Q: Which radical is least stable?
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Q: Which compound is more Stable? why?
A: Given, The structures are; Aromatic compounds are more stable than anti-aromatic and non-aromatic…
Q: Arrange the following compounds in order of stability by dragging them into the space below.
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Q: The following carbocations are listed in increasing order of stability (least to greatest stability)
A: Stability of carbocation can be explained by inductive effect Carbocations are electron deficient…
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: What is the correct order of stability of the following radicals (more stable > less stable)?
A:
Q: Assuming the rings are planar, which ions are aromatic? a. D. b. D:- d.
A: Aromatic compounds are the ones with cyclic planar ring and delocalization of pi electrons and…
Q: Which of the following is the least reactive diene?
A: We know that, Reactivity of diene can be increased by substituting electron withdrawing group. In…
Q: list the given dienes in the order from least reactive to most reactive.
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Q: Consider electrophilic aromatic substitution at the para position of anisole (R = OMe) and…
A: Wheland intermediate formed in Electrophilic substitution reaction.
Q: a. Rank the follow radicals from least to most stable. CH3 CH3 CH3 .F A B C D Now, explain…
A: Radical is a electron deficient species. Any electron donating group stabilize it and electron…
Q: Rank the following radicals in order of decreasing stability. most stable least stable (CHдС-снсн,…
A: Free radicals are electron deficeint. the stability of tertiary radicals is more than that of…
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: Between the following radicals; which one is more stable? I or II PHHC(*)CH2ET (1) PHCH2C(*)HEt (1I)…
A: Given free radicals are PhHC(•)CH2Et (I) PhCH2C(•)HEt (II) The free radical with more…
Q: Rank the carbocations in the Figure below in order of decreasing stability. ["~" = approximately…
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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: Rank the following carbocations in order of decreasing stability. Most stable
A: Carbocations are electron-deficient species that are formed by the removal of a hydrogen atom from…
Q: Which one is more stable S2-, S4-, S6-?
A: The given ions of Sulphur are S2-, S4-, and S6-.
Q: Given the compounds below, which is the more stable one?
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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: Rank the following free radicals in order of increasing stability I II III IV
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Q: Explain the Stability of Allylic Carbocations ?
A: Carbocations are positively charged, sp2 hybridized trigonal planer structures. They are electron…
Q: Explain why CH3CH2CH2CH2Cl reacts with 0.01M NaCN in Ethanol (C2H5OH) to yield primarily…
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Q: Investigating How Stereochemistry Affects Reactivity?
A: The product of a reaction is determined the stereochemistry of reactants and reagents.
Q: %3D
A: Resonance is defined as delocalization of pie electron . Electrons are flowing from high density to…
Q: Draw all important contributing structures for the following allylic carbocations; then rank the…
A: The carbocations are stabilized by more substitution, so the secondary carbocation is more stable…
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: Rank the following alkenes in order of increasing stability (least to most stable)
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Q: Rank the following radicals in order of increasing stability.
A: Since the stability of free radicals depends on two things 1) resonance => more is the resonance…
Q: I II III
A: We have to rank the following given carbanions in order of increasing stability as follows in step…
Q: Rank the following free radicals in order of increasing stability:
A: The highly reactive neutral intermediate species with one unpaired electron is known as radical. The…
Q: Which one is the most stable?
A: The more substituents the alkenes have, the more stable they are. Thus, a tetra substituted alkene…
Q: Draw out both reactants and the Diels-Alder products from reaction of the followin a. furan and…
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Q: Which of the following radicals are allylic? B D. only D A, B, and C B and C
A: The radicals given are,
Q: List them in order of stability from higher to lower
A: The order for the stability of the carbocation - Conjugated carbocation > tertiary carbocation…
Q: a. The reaction shown takes place in four steps. Complete the mechanism by adding curved arrows for…
A:
Q: Rank the free radicals shown below in order of increasing stability:
A:
Q: Write with additional resonance contributing structure for each carbocation and state which of the…
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Q: Order the numbered bonds in increasing order of dissociation energy.
A: Given : Different type of molecules. To find : order of bond dissociation energy. Solution : As we…
Q: Rank the following radicals in order of increasing stability.
A: The stability of free radical is governed by various factors such as: Allylic / benzylic radical 3°…
Q: Under what circumstances can you assume that the less stable of two compounds is the more reactive…
A: Compound with less energy is more stable. More reactive compound will be less stable, it depends on…
Q: Question attached
A: To determine the most stable compound from the below two compounds.
Q: Classify the following carbocations as primary, secondary, tertiary, methyl, or vinyl carbocations…
A: We have to predict the type of carbocation.
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- Classify the radicals into the appropriate categories. Primary, Secondary, Tertiary, AllylicWrite a line formula for all the free radicals that have the formula C5H11 and classify each as primary, secondary, or tertiary. Which one is the most stable?Using the table of average bond dissociation enthalpies at 25°C, determine which of the following reactions are energetically favorable at room temperature. Assume that ▲S = 0. Q. CH2=CH2 + CHI3 --> CH3CH2CI3
- Using the table of average bond dissociation enthalpies at 25°C, determine which of the following reactions are energetically favorable at room temperature. Assume that ▲S = 0. Q.CH2=CH2 + 2H2 + N2 --> H2NCH2CH2NH2Arrange the following radicals in order of increasing stability. Oka XList the following in order of decreasing (most to least ) stability Thanks!
- Decide whether each of the molecules in the table below is stable, in the exact form in which it is drawn, at pH = 2. If you decide at least one molecule is not stable, then redraw one of the unstable molecules in its stable form below the table. (If more than one molecule is unstable, you can pick any of them to redraw.) OH Ostable O unstable O stable O unstable OH OH u Ostable O unstable O stable O unstable 0 AJ :0 Ahm X trRank the radicals in order of decreasing stability. Most stable H3C- H3C- Looot otobloOrder these according to decreasing stability; 1 being the most stable, 4 the least stable. A B C D