Answer: All organic compound depends on H-bonding with water. more stronger H-bonding with water more will be soluble.
Explanation:
1. It depends primarily upon the function groups of that compound. It also depends on the size of the compound.
2. some organic compound which soluble in water for example: alcohols, ethers, carboxylic acids. Because of the functional groups attached to the organic structure (the C-H backbone) are what effect the solubilities.Like carboxylic acids and alcohols form hydrogen bonds with the water, helping to solubilize it.
3. Take alcohols for example: methanol, ethanol, and isopropanol are all completely soluble in water. By the time you get to butanol and some of the larger alcohols, including those with more complex structures, they tend to be less soluble.
1) The forward reaction is N2 (g) + O2 (g) → 2NO
(that reaction requires special contitions because at normal pressures and temperatures N2 and O2 do not react to form another compound.
2) The equiblibrium equation is
N2 (g) + O2 (g) ⇄ 2NO
3) Then, the reverse reaction is
2NO → N2(g) + O2(g)
Answer: 2NO → N2(g) + O2(g)
<span>The light spectrum that results from the light produced by an excited electron moving from a higher energy level back down to a lower energy level is an emission spectrum. The emission spectrum is formed by the electromagnetic radiation released by the transition in energy state.</span>
Nucleotide bases bonded to a sugar phosphate backbone make up nucleic acids such as DNA (deoxyribonucleic acid) and RNA (<span>ribonucleic acid)</span>. Nucleotides have three major parts: sugars, phosphates, and a nitrogenous base. DNA uses four nitrogenous bases: Adenine, Guanine, Cytosine, and Thymine. RNA uses the same bases except for Thymine, which is replaced by Uracil.
