Table of Contents
- 1 What are ortho and para directing groups Class 11?
- 2 Which is ortho and para directing group in electrophilic substitution reaction of benzene?
- 3 Which of the following group is ortho and para directing?
- 4 Which one of the following is ortho and para directing group in benzene?
- 5 What does ortho and para directing mean in organic chemistry?
What are ortho and para directing groups Class 11?
Some groups direct the second incoming group to the ortho and para positions simultaneously. These groups are called ortho-para directors. For example, when aniline is chlorinated, the product so obtained is ortho and para. The (-NH2) group directs the incoming group -Cl to ortho and para positions on the ring.
Why EDG are ortho and para directing?
Anilines, phenols, and ethers (such as anisole) However, the other effect called resonance add electron density back to the ring (known as the +M effect) and dominate over that of inductive effect. Hence the result is that they are EDGs and ortho/para directors.
Which is better ortho or para?
Here, we are being asked to compare the stability of the para and ortho hydrogen. – These two forms of molecular hydrogen are also referred to as spin isomers. – Now, due to antiparallel spin arrangement, para hydrogen has less energy and thus, they are more stable than ortho hydrogen.
Which is ortho and para directing group in electrophilic substitution reaction of benzene?
Electron donating groups like OH- donates some of its electron density to benzene ring through resonance. Hence position number 2,4,6(ortho/para) become electron rich and an electrophile can attack these positions easily. So EDG are ortho/para directing.
Which of the following group is ortho para directing?
−OH group is ortho and para directing due to resonance the electron density is more on ortho and para positions.
What is ortho position in chemistry?
Ortho position in organic chemistry is the one in which there are two same functional groups, tied to a ring of benzene in the positions 1 and 2. The abbreviation o- is used, for example, o-Hydroquinone is 1,2-dihydroxybenzene.
Which of the following group is ortho and para directing?
What is ortho meta and para in chemistry?
The terms ortho, meta, and para are prefixes used in organic chemistry to indicate the position of non-hydrogen substituents on a hydrocarbon ring (benzene derivative). The prefixes derive from Greek words meaning correct/straight, following/after, and similar, respectively.
Which of the following is ortho and para director group in benzene?
-The hydroxyl group is the strongest ortho para directing group as hydroxyl group is electron releasing group and it increases the electron density in the benzene ring through resonance and activates the ring towards electrophilic substitution. -Thus, among the following the strongest ortho para directing group is –OH.
Which one of the following is ortho and para directing group in benzene?
Which of the following is not an ortho para directing group?
\[-Na \to – C\] is not an ortho-para directing group.
What is the difference between ortho and para directing and meta directing?
Ortho, para directing groups are electron-donating groups; meta directing groups are electron-withdrawing groups. The halide ions, which are electron-withdrawing but ortho, para directing, are the exception.
What does ortho and para directing mean in organic chemistry?
If a particular group activates the nucleus and is ortho and para directing means then it does not mean that it will direct the new entrant only to ortho and para and that there will be no meta substituted compound is formed. In fact, the groups activating the nucleus form ortho and para compounds are formed in greater proportion than meta.
Is Nitro a para or ortho directing group?
eg. 2: Thus, the nitro group is a meta directing group. Ortho, para directing groups are electron-donating groups; meta directing groups are electron-withdrawing groups.
What are ortho and para directing groups in benzene?
Ortho, para-directing groups are groups whose presence in the benzene ring activates it for further electrophilic substitution. The second substitution takes place at the ortho and para (2, 4, 6) positions in relation to the first substituent already present in the ring.