Primary alkyl halides tend to undergo the SN2 reaction mechanism in nucleophilic substitution since there is less steric hindrance for nucleophilic attack and the carbocations that they form are not as stable as those formed from tertiary alkyl halides.
1-bromopentane > 1-bromo 2-methylbutane > <span>1-bromo-3-methylbutane</span>> 2-bromo 2-methylbutane
Formation of ammonia by nitrogen and hydrogen is habers process wher 28g N2 results in formation of 34g NH3
so 35g N2 will form 34*35/28=42.5g NH3 where it given that reaction takes place in excess of H2
N2+3H2 gives 2NH3
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↪1) Aqueous Solution
↪2) Solvent
↪3) Solute
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