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.
Answer:
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Explanation:
Answer
A. It changes the rate, R
Explanation
When we change the concentration of the reactants in a chemical reaction, it affects the rate of reaction that happens in the process. Typically, the rate of reaction will decrease with time if the concentration of the reactants decreases because the reactants will be converted to products. Similarly, the rate of reaction will increase when the concentration of reactants are increased.
Answer:
Ha is more acidic than Hb because loss of Ha forms a resonance-stabilized conjugate base.
Explanation:
The carbon atom that is next to the carbonyl group in pentan-2-one is known as the alpha carbon atom, this carbon atom bears the Ha, the alpha hydrogen atoms.
Ha is more acidic than Hb because, loss of Ha leads to the formation of a resonance stabilized enolate ion. This resonance stabilization of the ion formed makes loss of Ha an easier process than loss of Hb, hence the answer above.
Yes because molecules is solid
