The least Stable carbocation is

Q: Explain the attached statement is true or not ?

A: Given:

Q: Rank the carbocation compounds below from most stable to least stable.

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Q: QUESTION 1 Circle the best dienophile CH3

A: In Diels-Alder reaction dienophile is the 2pi system .

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: Which of the following carbocations is least likely to rearrange? +) A B D

A: Carbocation rearrangement takes place where there is a chance of transforming a less stable…

Q: c) What is the "order of stability"(most to least) of carbocations? Use the following list. methyl…

A: Tertiary Benzyl > Secondary Benzyl > Primary Benzyl > Secondary Diallyl > Primary Allyl…

Q: Step 2: Draw curved arrows to give elimination. : 0 MC HC ة CH CH₂ ا H H3C CH2 mayor. CH3 H H H

A: We have to show the mechanism for curved arrows.

Q: LEAST stable

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Q: Which molecule is more acidic? In fact, the more acidic molecule is roughly as acidic as water! H H…

A: Acidic character in the case of Bronsted acid is a molecule that can dissociate into negatively…

Q: Consider the following set of carbocations and answer the questions that follow. A в i. The…

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Q: two examples each of Unsymmetrical alkenes and reagents

A: Alkenes having different groups attached to either end of the carbon - carbon double bond are called…

Q: What is the major product of the reaction at the photo?

A: In an aromatic nucleophilic substitution reaction, a nucleophile attacks on the carbon atom of the…

Q: Place from high stability to lowest stability for  2,4 dimethyl pentane

A: The stability of any compound is inversely proportional to the steric repulsion between the groups…

Q: What reagent/reagents is/are necessary to transform the starting molecule into the desired product?…

A: The reaction is carried by Sandmeyer's reaction  Diazotisation of aniline followed by cuprous…

Q: Add the appropriate & and ô* symbols for all polar bonds in the following structures. 8. Н Н

A: The more electronegative atom has partial negative charge and the less electronegative atom has…

Q: Label the most stable and the second most stable carbocation. HOHO

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Q: A в Which of the alkenes above is the least stable (highest in energy)? Which is the most stable…

A: More substituted alkene is more stable. Alkyl group is electron donating and it stabilize alkene

Q: ose the best starting alkyne for the reaction in the im

A: Various organic compounds are converted to other organic compounds with the help of some reagents.

Q: Which statement(s) is/are true regarding leaving Broups? L Weak bases make good leaving groups. II.…

A: I . ) Good leaving groups are weak bases. They're happy and stable on their own. Some examples of…

Q: among the two product which is the correct answer?

A: The correct answer is

Q: OCH3

A:

Q: Which alkene is lower in energy? O The alkene on the left is lower in energy The alkene on the right…

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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: What would be the steps needed to transform the first molecule into the second molecule?

A: On bromination in the presence of light, methylcyclopentane is converted to…

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: Rank order the following in terms of relative reactivity (most reactive on the left, least reactive…

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Q: Draw the most stable carbocation that can be formed by the compound in Figure 5.

A: A carbocation is for when a carbon atom acquires a positive charge, The shape of a carbocation is…

Q: b. С. + + + a.

A: The reactive intermediate species in which carbon atom forms only three bonds and contains a…

Q: The inductive effect stabilizes carbocations and carbon radicals. primary secondary tertiary O all…

A: Inductive effect : It is the tendency of releasing/withdrawing electron in a bond by an atom or…

Q: What type of carbocation is shown? (+)

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Q: 1. CH3 H3C-C. CH3 :Br r-Br: CH3 H3C-C-Br: I CH3 Br:

A:

Q: The

A: Ketone react with ethanol then we get acetal product. First ketone protonated by the gain of H+ then…

Q: ng carbocations

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Q: Both questions help please 1) ‘When a hydrogen halide adds to an asymmetrical alkene, the addition…

A: IUPAC nomenclature of organic chemistry is a method of naming organic chemical compounds

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: Part 3 out of 4 Select the compound that results from the reaction with following resonance…

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Q: For each of the alkyl bromides, do think it is likely to form the you substitution or elimination…

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Q: Which carbocation is more stable? Briefly explain why. A B Ph, + Ph Ph Ph

A: Since, We know that, More is the resonating structure , more will be the stable carbocation formed.

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: Rank the following from most reactive to least reactive in an SN1 reaction.

A: Since the reactivity of SN1 reaction depends on the stability of the carbocation formed after…

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: Explain why1-bromobicyclo [2.2.2] octane is not likely to undergo an Sn1 or an SN2 substitution…

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Q: In the molecules below, circle the carbon that will most likely have the electrophile attached to it…

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Q: When a is on an atom directly attached to a benzene ring, the benzene ring will stabilize it by…

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Q: What type of carbocation is shown?

A: As we can clearly see that the positive charge (cation) containing carbon is attached to two carbon…

Q: 1=first in name 4%=last in name

A: write the position numbers and names of the substituent groups, in alphabeticalorder, before the…

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

A: While writing mechanism, curved electron pushing arrow to be shown from negatively charged…