Which of the following is not a possible reaction of a carbocation? (a) addition of a nucleophile (b) rearrangement to a more stable carbocation (c) addition of a proton to form an alkane (d) loss of a β-hydrogen to form an alkene

Which of the following is not a possible reaction of a carbocation?
(a) addition of a nucleophile
(b) rearrangement to a more stable carbocation
(c) addition of a proton to form an alkane
(d) loss of a β-hydrogen to form an alkene
by

1 Answer

Answer :

addition of a proton to form an alkane
by

Related questions

Which of the following is not a correct statement about the electrophilic substitution mechanism of benzene? (a) Benzene functions as a nucleophile. (b) Formation of a carbocation intermediate is the rate-determining step. (c) The carbocation intermediate contains an sp3 hybridized carbon in the ring. (d) The addition product is a frequently observed minor product.

Description : Which of the following is not a correct statement about the electrophilic substitution mechanism of benzene? (a) Benzene functions as a nucleophile. (b) Formation of a carbocation intermediate is the ... hybridized carbon in the ring. (d) The addition product is a frequently observed minor product.

Last Answer : The addition product is a frequently observed minor product.

The higher reactivity of an alkene or alkyne, as compared to an alkane, is due to (a) sigma bonds (b) pi bonds (c) hydrogen bonds (d) None of these

Description : The higher reactivity of an alkene or alkyne, as compared to an alkane, is due to (a) sigma bonds (b) pi bonds (c) hydrogen bonds (d) None of these

Last Answer : pi bonds

A compound of formula C6H12 does not react with concentrated sulfuric acid. The compound could be (a) Alkane (b) Cycloalkane (c) Alkene (d) Cycloalkene

Description : A compound of formula C6H12 does not react with concentrated sulfuric acid. The compound could be (a) Alkane (b) Cycloalkane (c) Alkene (d) Cycloalkene

Last Answer : Cycloalkane

A compound reacts with steam in the presence of concentrated H2SO4 to give isopropyl alcohol. The compound could be (a) Alkane (b) Alkyne (c) Alkene (d) Allene

Description : A compound reacts with steam in the presence of concentrated H2SO4 to give isopropyl alcohol. The compound could be (a) Alkane (b) Alkyne (c) Alkene (d) Allene

Last Answer : Alkene

A compound of formula C3H8 does not react with bromine in CCl4 in the dark. The compound could be (a) Alkane (b) Cycloalkane (c) Alkene (d) Cycloalkene

Description : A compound of formula C3H8 does not react with bromine in CCl4 in the dark. The compound could be (a) Alkane (b) Cycloalkane (c) Alkene (d) Cycloalkene

Last Answer : Alkane

Which of the following organic compounds is known as a saturated chain hydrocarbon ? w) an aromatic compound x) an alkene y) an alkyne z) an alkane

Description : Which of the following organic compounds is known as a saturated chain hydrocarbon ? w) an aromatic compound x) an alkene y) an alkyne z) an alkane

Last Answer : ANSWER: Z -- AN ALKANE

CONDENSED STRUCTURE OF THE FOLLOWING1. 5,5 – diethyl – 3,3 – dimethyl – 1 - octyne2. 2,4,4,6 – tetraethyl – 3,3 – nondiene3. 1,1,4,4 – tetramethylheptaneIDENTIFY IF ITS ALKANE ALKYNE ALKENE?

Description : CONDENSED STRUCTURE OF THE FOLLOWING1. 5,5 – diethyl – 3,3 – dimethyl – 1 - octyne2. 2,4,4,6 – tetraethyl – 3,3 – nondiene3. 1,1,4,4 – tetramethylheptaneIDENTIFY IF ITS ALKANE ALKYNE ALKENE?

Last Answer : ℤ.

Classify the following into saturated and unsaturated hydrocarbons – Benzene, cyclopropane, alkene and alkane, methane, ethene, Propyne, butene

Description : Classify the following into saturated and unsaturated hydrocarbons – Benzene, cyclopropane, alkene and alkane, methane, ethene, Propyne, butene

Last Answer : Saturated: Alkane, cyclopropane, methane Unsaturated: Benzene, alkene, ethene, Propyne, butene

Why does a H+ ion attacking a carbon-carbon double bond add to the carbon with the least number of substituents? (a) the reaction is resonance stabilized. (b) the hybrid geometry favors this process. (c) nucleophile tends to attack stable centers of negative charge. (d) a more stable carbonium ion is generated.

Description : Why does a H+ ion attacking a carbon-carbon double bond add to the carbon with the least number of substituents? (a) the reaction is resonance stabilized. (b) the hybrid geometry favors this ... tends to attack stable centers of negative charge. (d) a more stable carbonium ion is generated.

Last Answer : a more stable carbonium ion is generated.

The hydroboration-oxidation reaction can be characterized as the _________ to an alkene. (a) anti-Markovnikov syn addition of water (b) anti-Markovnikov anti addition of water (c) Markovnikov syn addition of water (d) Markovnikov anti addition of water

Description : The hydroboration-oxidation reaction can be characterized as the _________ to an alkene. (a) anti-Markovnikov syn addition of water (b) anti-Markovnikov anti addition of water (c) Markovnikov syn addition of water (d) Markovnikov anti addition of water

Last Answer : anti-Markovnikov syn addition of water

Pick out the wrong statement. (A) The nucleus of a hydrogen atom is identical with a proton (B) A, β-ray particle is identical with an electron (C) Mass of an electron is about 1/1800th of the lightest nucleus (D) Positron is heavier than a proton

Description : Pick out the wrong statement. (A) The nucleus of a hydrogen atom is identical with a proton (B) A, β-ray particle is identical with an electron (C) Mass of an electron is about 1/1800th of the lightest nucleus (D) Positron is heavier than a proton

Last Answer : (D) Positron is heavier than a proton

Which is most stable carbocation?

Description : Which is most stable carbocation?

Last Answer : Which is most stable carbocation? A. n-Propyl cation B. Isopropyl cation C. Ethyl cation D. Triphenylmethyl cation

Most stable carbocation is:

Description : Most stable carbocation is:

Last Answer : Most stable carbocation is: A. B. C. D.

Most stable carbocation is:

Description : Most stable carbocation is:

Last Answer : Most stable carbocation is: A. `CH_(3)-overset(+)CH_(2)` B. `overset(+)CH_(2)CHCl_(2)` C. `overset(+)CH_ ... (2)Cl` D. `overset(+)CH_(2)-CH_(2)NO_(2)`

The most stable carbocation is :

Description : The most stable carbocation is :

Last Answer : The most stable carbocation is : A. methyl carbocation B. primary carbocation C. secondary carbocation D. tertiary carbocation

Why do aldehydes undergo nucleophilic addition reactions while esters undergo nucleophilic acyl substitution reactions? (a) The carbonyl carbon of an ester is more electrophilic than that of an aldehyde. (b) Aldehydes are more sterically hindered than esters. (c) Once the nucleophile adds to an aldehyde, the tetrahedral intermediate is too sterically hindered to eliminate one of the attached groups. (d) Once the nucleophile adds to an aldehyde, neither H− nor R− can be eliminated since they are strongly basic

Description : Why do aldehydes undergo nucleophilic addition reactions while esters undergo nucleophilic acyl substitution reactions? (a) The carbonyl carbon of an ester is more electrophilic than that of an aldehyde. (b) ... adds to an aldehyde, neither H− nor R− can be eliminated since they are strongly basic

Last Answer : Once the nucleophile adds to an aldehyde, neither H− nor R− can be eliminated since they are strongly basic

Which of the following statements correctly describes the general reactivity of alkynes? (a) An alkyne is an electron-rich molecule and therefore reacts as a nucleophile. (b) The σ bonds of alkynes are higher in energy than the bonds and are thus more reactive. (c) Unlike alkenes, alkynes fail to undergo electrophilic addition reactions. (d) Alkynes are generally more reactive than alkenes.

Description : Which of the following statements correctly describes the general reactivity of alkynes? (a) An alkyne is an electron-rich molecule and therefore reacts as a nucleophile. (b) The σ bonds ... fail to undergo electrophilic addition reactions. (d) Alkynes are generally more reactive than alkenes.

Last Answer : Alkynes are generally more reactive than alkenes.

Which of the following is the most stable alkene? (a) trans-3-hexene(b) cis-3-hexene(c) 1-hexene(d) (Z)-3-hexene

Description : Which of the following is the most stable alkene? (a) trans-3-hexene (b) cis-3-hexene (c) 1-hexene (d) (Z)-3-hexene

Last Answer : trans-3-hexene

With hydrocarbons, is chlorine the ONLY atom powerful enough to remove a hydrogen atom from an alkane?

Description : With hydrocarbons, is chlorine the ONLY atom powerful enough to remove a hydrogen atom from an alkane?

Last Answer : (Disclaimer: I had organic chemistry 10 years ago, so you may want to back this up with some googling) Flourine reacts with alkanes, but it is so reactive it is unpredictable; you don't know ... . It seems like you can get the more powerful acids to react with alkanes under the right conditions.

Alkene `A(Me_2 C = CMe_2)` is more stable than alkene `B(Et_2 C = Cet_2)`. Baker-Nathan effect.

Description : Alkene `A(Me_2 C = CMe_2)` is more stable than alkene `B(Et_2 C = Cet_2)`. Baker-Nathan effect.

Last Answer : Alkene `A(Me_2 C = CMe_2)` is more stable than alkene `B(Et_2 C = Cet_2)`. Baker-Nathan effect. A. If ... . D. IF (A) is incorrect but (R) is correct.

Conversion of pepsinogen to pepsin is (A) Intra molecular rearrangement (B) Breaking of hydrogen bonds (C) Covalent modification (D) Polymerisation

Description : Conversion of pepsinogen to pepsin is (A) Intra molecular rearrangement (B) Breaking of hydrogen bonds (C) Covalent modification (D) Polymerisation

Last Answer : Answer : C

True or False: A chemical reaction is the rearrangement of atoms you start with to form new compounds?

Description : True or False: A chemical reaction is the rearrangement of atoms you start with to form new compounds?

Last Answer : TRUE

Which of the following statements concerning SN2 reactions of alkyl halides is not correct? (a) The rate of reaction depends on the concentration of the nucleophile. (b) The rate of reaction depends on the concentration of the alkyl halide. (c) The rate of reaction of a particular alkyl bromide depends on the steric accessibility of the carbon of the C-Br bond. (d) All alkyl iodides react more rapidly than all alkyl chlorides

Description : Which of the following statements concerning SN2 reactions of alkyl halides is not correct? (a) The rate of reaction depends on the concentration of the nucleophile. (b) The rate of reaction depends on the ... carbon of the C-Br bond. (d) All alkyl iodides react more rapidly than all alkyl chlorides

Last Answer : All alkyl iodides react more rapidly than all alkyl chlorides

Phenol is more reactive than benzene towards electrophilic substitution reaction. In case of Phenol, the intermediate carbocation is more resonance st

Description : Phenol is more reactive than benzene towards electrophilic substitution reaction. In case of Phenol, the intermediate carbocation is more resonance st

Last Answer : Phenol is more reactive than benzene towards electrophilic substitution reaction. In case of Phenol, the ... D. A is incorrect but R is correct

Which of the following factors influence whether a reaction will proceed by an SN1, SN2, E1, or E2 mechanism? (a) Structure of the alkyl halide (b) Solvent (c) Concentration of reagents (d) Nature of the nucleophile (e) All of these

Description : Which of the following factors influence whether a reaction will proceed by an SN1, SN2, E1, or E2 mechanism? (a) Structure of the alkyl halide (b) Solvent (c) Concentration of reagents (d) Nature of the nucleophile (e) All of these

Last Answer : All of these

In the reaction of propene with HCl, H+ ion acts as the : (a) electrophile (b) carbonium ion (c) nucleophile (d) carbanion

Description : In the reaction of propene with HCl, H+ ion acts as the : (a) electrophile (b) carbonium ion (c) nucleophile (d) carbanion

Last Answer : electrophile

Which of the following reaction mechanism doe not involves carbocation as an intermediate ?

Description : Which of the following reaction mechanism doe not involves carbocation as an intermediate ?

Last Answer : Which of the following reaction mechanism doe not involves carbocation as an intermediate ? A. ... C. Fries Rearrangements D. Diels- Alder reaction

Carbocation as an intermediate is likely to be formed in the reaction :

Description : Carbocation as an intermediate is likely to be formed in the reaction :

Last Answer : Carbocation as an intermediate is likely to be formed in the reaction : A. `"Hexene"overset("Anhyd ... + HCN"overset(.^(-)OH)rarr"acetonecyanohydrin"`

Carbocation is a reaction intermediate in which of the following reactions?

Description : Carbocation is a reaction intermediate in which of the following reactions?

Last Answer : Carbocation is a reaction intermediate in which of the following reactions? A. `E_(1)` reactions B. ... ^(1))` reaction D. All of the above

Pick out the correct statement. (A) Positron is the antiparticle of electron (B) In α-decay, the ratio of neutron to proton decreases (C) Ionising power of β-rays is higher than that of α-rays (D) Speed of α-rays is more than that of γ-ray

Description : Pick out the correct statement. (A) Positron is the antiparticle of electron (B) In α-decay, the ratio of neutron to proton decreases (C) Ionising power of β-rays is higher than that of α-rays (D) Speed of α-rays is more than that of γ-ray

Last Answer : (A) Positron is the antiparticle of electron

The disappearance of the purple color of KMnO4 in its reaction with alkene is known as (a) Markovnikov test (b) Grignard test (c) Baeyer test (d) Wurtz test

Description : The disappearance of the purple color of KMnO4 in its reaction with alkene is known as (a) Markovnikov test (b) Grignard test (c) Baeyer test (d) Wurtz test

Last Answer : Baeyer test

A radioactive substance does not emit (A) α-ray (B) Proton (C) Position (D) β-ray

Description : A radioactive substance does not emit (A) α-ray (B) Proton (C) Position (D) β-ray

Last Answer : (B) Proton

In β-decay of radioactive material, the ratio of neutron to proton (A) Increases (B) Remain same (C) Decreases (D) Is unpredictable; may increase or decrease

Description : In β-decay of radioactive material, the ratio of neutron to proton (A) Increases (B) Remain same (C) Decreases (D) Is unpredictable; may increase or decrease

Last Answer : (C) Decreases

___________ remain undeflected in a magnetic field a) β particles b) α particles c) γ rays d) Proton beams

Description : ___________ remain undeflected in a magnetic field a) β particles b) α particles c) γ rays d) Proton beams

Last Answer : c) γ rays

Benzene undergoes substitution reaction more easily than addition reaction because (a) it has a cyclic structure (b) it has three double bonds (c) it has six hydrogen atoms (d) there is delocalization of electrons

Description : Benzene undergoes substitution reaction more easily than addition reaction because (a) it has a cyclic structure (b) it has three double bonds (c) it has six hydrogen atoms (d) there is delocalization of electrons

Last Answer : there is delocalization of electrons

Benzene undergoes substitution reaction more easily than addition reaction because (a) it has a cyclic structure (b) it has three double bonds (c) it has six hydrogen atoms (d) there is delocalization of electrons

Description : Benzene undergoes substitution reaction more easily than addition reaction because (a) it has a cyclic structure (b) it has three double bonds (c) it has six hydrogen atoms (d) there is delocalization of electrons

Last Answer : there is delocalization of electrons

--------rearrangement give the product of Cine substitution. a. Wittig b. Von Richter c. Rupe d. Lossen

Description : --------rearrangement give the product of Cine substitution. a. Wittig b. Von Richter c. Rupe d. Lossen

Last Answer : b. Von Richter

----rearrangement involves alpha diketone. a. Wolf b. Schmidt c. Hofmann d. Curtius

Description : ----rearrangement involves alpha diketone. a. Wolf b. Schmidt c. Hofmann d. Curtius

Last Answer : a. Wolf

Which of the following alkane is synthesised from single alkyl halide by wurtz reaction:-

Description : Which of the following alkane is synthesised from single alkyl halide by wurtz reaction:-

Last Answer : Which of the following alkane is synthesised from single alkyl halide by wurtz reaction:- A. B. C. D.

What is the name given for a species that contains a positively charged carbon atom? (a) carbanion (b) carbocation (c) methyl radical (d) free radical

Description : What is the name given for a species that contains a positively charged carbon atom? (a) carbanion (b) carbocation (c) methyl radical (d) free radical

Last Answer : carbanion

What happens in a reduction reaction? (1) addition of Oxygen (2) addition of Nitrogen (3) addition of Hydrogen (4) None of the above

Description : What happens in a reduction reaction? (1) addition of Oxygen (2) addition of Nitrogen (3) addition of Hydrogen (4) None of the above

Last Answer : (3) addition of Hydrogen Explanation: In terms of Oxygen transfer, oxidation is gain of oxygen; reduction is loss of oxygen. However, in terms of hydrogen transfer, oxidation is loss of hydrogen, reduction is gain of hydrogen.

Which one of the following has greatest mass? (1) electron (2) proton (3) neutron (4) hydrogen nucleus

Description : Which one of the following has greatest mass? (1) electron (2) proton (3) neutron (4) hydrogen nucleus

Last Answer : (3) neutron

The atomic number of hydrogen is 1. This implies that it contains _______ in its Kshell. (1) One neutron (2) One proton (3) One electron (4) None of the above

Description : The atomic number of hydrogen is 1. This implies that it contains _______ in its Kshell. (1) One neutron (2) One proton (3) One electron (4) None of the above

Last Answer : (3) One electron Explanation: This implies that Hydrogen has one electron in its K shell. Also, it requires one more electron to fill the K shell. So two hydrogen atoms share their electrons to form a molecule of hydrogen, H2.

The radioactive isotope of hydrogen is called--------- and its nucleus contains --------proton and --- --neutron.

Description : The radioactive isotope of hydrogen is called--------- and its nucleus contains --------proton and --- --neutron.

Last Answer : Ans: Tritium, one and two

Which one of the following has greatest mass ? (1) electron (2) proton (3) neutron (4) hydrogen nucleus

Description : Which one of the following has greatest mass ? (1) electron (2) proton (3) neutron (4) hydrogen nucleus

Last Answer : neutron

What is the name of the simplest alkane ?

Description : What is the name of the simplest alkane ?

Last Answer : The simplest alkene is methane.

Which of the following produces highest amount of energy upon oxidation? (1) Protein (2) Fat (3) Glucose (4) An alkane

Description : Which of the following produces highest amount of energy upon oxidation? (1) Protein (2) Fat (3) Glucose (4) An alkane

Last Answer : (2) Fat Explanation: Fats consist of a wide group of compounds that are generally soluble in organic solvents and generally insoluble in water. Chemically, fats are triglycerides, triesters of glycerol and ... while "fats" is usually used to refer to fats that are solids at normal room temperature.

What effect does branching of an alkane chain has on its boiling point?

Description : What effect does branching of an alkane chain has on its boiling point?

Last Answer : Ans. As branching increases, the surface area of the molecule decreases which results in a small area of contact. As a result, the Van der Waals force also decreases which can be overcome at ... lower temperature. Hence, the boiling point of an alkane chain decreases with an increase in branching.

(a) What effect the branching of an alkane has on its melting point? (L-III) (b) Which of the following has highest boiling point?(L-III) (1) 2-methyl pentane. (2) 2, 3-diethyl butane. (3) 2, 2- dimethyl butane.

Description : (a) What effect the branching of an alkane has on its melting point? (L-III) (b) Which of the following has highest boiling point?(L-III) (1) 2-methyl pentane. (2) 2, 3-diethyl butane. (3) 2, 2- dimethyl butane.

Last Answer : Ans.(a) In general conception, as the branching increases packing of the molecules in the crystals becomes less close and have melting point decreases accordingly. (b) As the branching increases, ... attraction decreases and hence the boiling point decreases. So, 2-methyl pentane has highest B.pt.

What effect does branching of an alkane chain has on its boiling point?

Description : What effect does branching of an alkane chain has on its boiling point?

Last Answer : Ans. As the branching increases, the surface area of an alkane approaches that of a sphere. Since a sphere has minimum surface area, therefore, Vander Waal forces of attraction are minimum and hence the boiling point of the alkane decreases with branching.