Answer:
1) HNO3/H2SO4, 2) CH3CH2CH2Cl/AlCl3
Explanation:
Benzene is a stable aromatic compound hence it undergoes substitution rather than addition reaction.
When benzene undergoes substitution reaction, the substituent introduced into the ring determines the position of the incoming electrophile.
If I want to synthesize m-nitropropylbenzene, I will first carry out the nitration of benzene using HNO3/H2SO4 since the -nitro group is a meta director. This is now followed by Friedel Craft's alkykation using CH3CH2CH2Cl/AlCl3.
Answer:
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<em>sol</em><em>ution</em><em>,</em>
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<em>Now</em><em>,</em>
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<em>hope</em><em> </em><em>this </em><em>helps</em><em>.</em><em>.</em><em>.</em>
<em>Good</em><em> </em><em>luck</em><em> on</em><em> your</em><em> assignment</em><em>.</em><em>.</em><em>.</em><em>.</em>
Answer:
LOL i belive its 200 because i did this exact same thing yesterday for homework and got it right so yeah, it should work. if it doesnt im sorry! but yeah XD sub to my yt channel too! DB_PLAYS <3
Explanation:
A mole is the assemblage of 6.022×10^23 ions.This number is also known as Avogadro Number.
Avogadro constant=6.022×10^23 mol^-1
Specific events in virus replication identified as targets for antiviral agents are viral adsorption, penetration, uncoating, and viral nucleic acid synthesis as well as viral protein synthesis.