Answer:
As you move across a period the electrons are being added to the same shell. But, protons are being added as well. This makes the nucleus more positively charged and, increasing protons has a greater effect than electrons. So, there is a greater nuclear attraction and, because the electrons are being added to the same shell that shell gets pulled in more. This causes a decrease in atomic radius.
Explanation:
Answer:
See attachment.
Explanation:
Mono-substituted cyclohexanes are more stable with their substituents in an equatorial position. However, with poly-substituted cyclohexanes, the situation is more complex since the steric effects of all substituents have to be taken into account. In this case, you can see that <u>the interconversion is shifted towards the conformation in the bottom because there is less tension between the substituents</u>.
<span>
Phenobarbital is derivative of
Barbituric Acid and Barbituric Acid is derivative of
Urea. (structures shown in Fig below)
Urea has H</span>₂N- group attached to Carbonyl Group (C=O), and such class of comounds conataining H₂N-C=O bond are called as Amides.
Result: So, <span>Phenobarbital belongs to
Amides.</span>
The answer to your question is Gallium, or GA. The trick is to always check if they are along the same vertical column. This indicates that they have the same Valence electrons, which is involved in all the bonding and define the electronegative status of the atom.
Left side metals right side non metals. arrganged in groups (columns) and periods (rows), each group tells you amount of valence electrons