User Prajwal Tiwari

9 votes

2 answers

1k views

Determining if the product would be cis or trans after an anti elimination on fischer projections

asked Jun 17, 2021 at 11:56

9 votes

1 answer

254 views

Why does this ring contraction take place in the following nucleophilic substitution? [closed]

asked Jun 17, 2021 at 12:31

8 votes

1 answer

229 views

Does a reaction proceed through SN1 if rearrangement results in a stable carbocation?

asked May 17, 2021 at 18:16

8 votes

3 answers

825 views

Comparing the rates of hydrolysis of different haloalkanes

asked May 25, 2021 at 7:31

7 votes

1 answer

2k views

The reaction of Alkyl Halides with sodium nitrite in DMF

asked May 6, 2021 at 15:31

7 votes

1 answer

220 views

Analysing reaction with chair conformation of substituted cyclohexane

asked Jun 14, 2021 at 14:55

6 votes

1 answer

327 views

When does reaction of alcohol with alumina give an ether and when an alkene?

asked Jun 11, 2021 at 10:30

5 votes

1 answer

186 views

Characteristics of cations with KCN and excess KCN

asked Sep 10, 2021 at 6:36

5 votes

1 answer

2k views

Does boron form compounds without covalent bonds?

asked Dec 14, 2020 at 5:23

4 votes

1 answer

287 views

What would be the product (B) in the following sequence of reaction?

asked Apr 3, 2021 at 19:10

3 votes

0 answers

91 views

What happens when tran-2-butene reacts with aqueous bromine in the presence of chloride?

asked Mar 23, 2021 at 15:16

3 votes

1 answer

159 views

Relative acidity of acetic acid derivatives with strongly withdrawing substituents

asked Mar 9, 2021 at 20:25

3 votes

0 answers

410 views

How many equivalents of Grignard reagent does a nitrile group consume?

asked Jun 16, 2021 at 9:41

3 votes

2 answers

511 views

Why is Electron Gain Enthalpy of only Be and Mg positive, in group 2?

asked Jun 7, 2021 at 12:07

3 votes

1 answer

235 views

Determining the mechanism followed when alcohols undergo a reaction with sodium bromide and sulphuric acid

asked May 4, 2021 at 11:36

2 votes

1 answer

192 views

Choosing hyperconjugation when resonance doesn't give a reason for stability

asked Apr 12, 2021 at 4:03

2 votes

1 answer

292 views

Can Positive ions satisfy primary valences according to Werner's theory for coordination compounds?

asked Apr 11, 2022 at 6:08

2 votes

2 answers

3k views

Relative stability of $\ce{V^2+}$ and $\ce{V^3+}$ and their Standard Electrode Potential

asked May 2, 2022 at 4:16

2 votes

1 answer

203 views

Regioselectivity of SN2 reaction on adenine

asked Jul 6, 2022 at 4:35

1 vote

0 answers

77 views

Determining which of these has the maximum S-O Bond Length?

asked Nov 6, 2021 at 6:18

1 vote

0 answers

54 views

Determining the leaving group for substituted benzene in Aromatic nucleophilic substitution

asked Jun 16, 2021 at 10:06

1 vote

0 answers

306 views

Why is oxalic acid more acidic than benzoic acid?

asked Mar 31, 2021 at 12:24

1 vote

0 answers

112 views

In a pair of diastereomers, which of the following is true?

asked Apr 4, 2021 at 2:48

0 votes

1 answer

71 views

When is the n+l rule followed when working with energy of different orbitals?

asked Apr 8, 2021 at 8:37

0 votes

0 answers

34 views

How would we arrange these in the increasing order of stability? [duplicate]

asked Mar 18, 2021 at 13:32

0 votes

0 answers

439 views

Stabillity of ethyl, iso propyl and vinyl free radicals

asked Mar 19, 2021 at 13:34

0 votes

1 answer

370 views

What would be the major products of this reaction?

asked Mar 19, 2021 at 15:53

0 votes

1 answer

318 views

Applying the Pauling's electronegativity when the ionisation enthalpy and electron gain enthalpy of an element are given

asked Jun 1, 2021 at 2:18

0 votes

0 answers

56 views

Comparing stability of two carbocations [duplicate]

asked Sep 25, 2021 at 1:59

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29 Questions

Determining if the product would be cis or trans after an anti elimination on fischer projections

Why does this ring contraction take place in the following nucleophilic substitution? [closed]

Does a reaction proceed through SN1 if rearrangement results in a stable carbocation?

Comparing the rates of hydrolysis of different haloalkanes

The reaction of Alkyl Halides with sodium nitrite in DMF

Analysing reaction with chair conformation of substituted cyclohexane

When does reaction of alcohol with alumina give an ether and when an alkene?

Characteristics of cations with KCN and excess KCN

Does boron form compounds without covalent bonds?

What would be the product (B) in the following sequence of reaction?

What happens when tran-2-butene reacts with aqueous bromine in the presence of chloride?

Relative acidity of acetic acid derivatives with strongly withdrawing substituents

How many equivalents of Grignard reagent does a nitrile group consume?

Why is Electron Gain Enthalpy of only Be and Mg positive, in group 2?

Determining the mechanism followed when alcohols undergo a reaction with sodium bromide and sulphuric acid

Choosing hyperconjugation when resonance doesn't give a reason for stability

Can Positive ions satisfy primary valences according to Werner's theory for coordination compounds?

Relative stability of $\ce{V^2+}$ and $\ce{V^3+}$ and their Standard Electrode Potential

Regioselectivity of SN2 reaction on adenine

Determining which of these has the maximum S-O Bond Length?

Determining the leaving group for substituted benzene in Aromatic nucleophilic substitution

Why is oxalic acid more acidic than benzoic acid?

In a pair of diastereomers, which of the following is true?

When is the n+l rule followed when working with energy of different orbitals?

How would we arrange these in the increasing order of stability? [duplicate]

Stabillity of ethyl, iso propyl and vinyl free radicals

What would be the major products of this reaction?

Applying the Pauling's electronegativity when the ionisation enthalpy and electron gain enthalpy of an element are given

Comparing stability of two carbocations [duplicate]