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Chemistry: Post your doubts here!

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Is the second edition of the Cambridge endorsed Chemistry textbook (authors are Dawnie, Norris, David Acaster and maybe someone else) released yet?

Remember, SECOND EDITION - printed 2014, specifically for the new syllabus.
 
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What's the reason for Sodium and group 1 elements having a low melting point?
Doesn't answer her question. :p
princess Anu:

If by any chance you don't get what I have just wrote, then here is a simpler explanation

As we go down the group, the size of the atoms increases right? Thus the outer valence electron goes farther away from the nucleus (the nucleus is at the center). Metallic bonding involves the attraction between the valence of electrons and the nucleus. Since the valence electrons are farther away, there will be less attraction between the nucleus and the electrons. Kinda like a magnet and a strip of iron. The farther you take the strip from the magnet, the weaker the attraction. Since the attraction is weaker, less energy is required to overcome the forces of attraction.

The suggested answer, while conceptually correct, has not answered the question totally.

It's more of explaining why the melting point of Group I metals decreases down the group rather than why Group I metals on the whole has a low melting point.

To answer the second point, we need to bring in the fact that strength of metallic bonds are proportional to the number of delocalised electrons, and that Group I metals will only provide one electron per atom.

In summary, strength of metallic bond is directly proportional to delocalised electrons and indirectly proportion to atomic radii.
 
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ull get CO2. u can also have it in a carbonate compound. depending on the reagent added like KOH or NaOH (any basic). since here NaOH was used so it can be NaCO3

Ans: NaCO3 /CO2
since there is an amine group due to hydrolysis(breaking bonds) it'll break apart n be in ion state or can be in amine compound which r stable enough.
so it may be CH3NH3+ Cl- or CH3NH2 (amine)

moreover, theres the aryl group there. so due to hydrolysis...the R group is seperated leaving the aryl group. i wont call it phenol exactly coz theres 2 rings joined there. so generalising it ...it becomes an aryl


in short answer : CH3NH3+Cl- and CO2 and the aryl with a phenol nxt to it (means one ring will have OH group on carbon 1)
 
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