"OH" group attached to aromatic ring is electrons donor because it has two lone pairs of electrons on oxygen atom which may involve in resonance process, but "OH" group attached to saturated carbon act as electrons attracting group due to high electronegativity of oxygen.
Radical
For the particles in the atom: Neutron: James Chadwick, 1932 Electron: J. J. Thomson, 1897 Proton: Ernest Rutheford, 1919
oh oh u have to go to the hospital fast ....u got the drips
Ferric means iron is in the +3 state; hydroxide means the anion is the OH- ion. So the whole formula is Fe(OH)3.
A picometer (pm) is equal to 1 x 10^-12 m. The O-H bond lengths in water are 95.8 pm,while S-H bond lengths in dihydrogen sulfide are 135 pm. Why are S-H bonds longer than O-H bonds? Is it because Sulfurs mass is greater than Oxygens mass? Please correct me if I'm wrong. Oxygen = 15.99 Sulfur = 32.06
Substituents with a negative Hammet substituent constant are electron donating. Examples include R groups and OH groups.
Arrhenius bases produce OH- ions by definition when dissolved in water. A Bronsted - Lowry base can produce OH- ions, but only has to produce a proton accepting group by definition. A Lewis base is defined as an electron donating group, which hydroxide ion is. So, basic compounds do produce OH- ions when dissolved in water, but not in all cases.
The base in a chemical reaction is the species that either (a) accepts a proton, (b) produces an OH- ion, or (c) is an electron donor.
nitro group is very electronegative,so it withdraws electron from the benzene ring so as to destabalize the carbocations in the ortho- and para- position. Nitro group is also fairly bulky so steric hinderance limits the formation of ortho product.ok?
Phenols are acidic in aqueous solution. The oxygen atom off of the benzene ring acts as an electron donating group, and pulls the electron density towards the benzene ring and away from the hydrogen atom. This makes the hydrogen easily extracted by free floating H2O molecules. Because of this, H3O+ molecules form, and this is equivalent to H+ which can show a low pH, which is characteristic of acidic solutions.
Hydroxyl group, -OH
When a bond in water molecule H20 breaks it forms H+ and OH-. The extra electron comes from H. H-O-H ------> H+ + OH-
The -OH group is called the hydroxyl group
Aldehydes and ketones haven't an -OH group.
hydroxyl
The hydroxyl group (-OH) is the functional group that defines alcohols.
OH groups a strongly electron withdrawing. The effect of two of these groups on a single carbon is that it causes de-shielding of the carbon nucleus making the carbon atom a strong electrophile. The carbon then attacks the lone pair of one of the hydroxyl groups, forming a C, O double bond and expelling a proton and a hydroxide ion which form water.