CHvaryангиansQue soven 3ΜΟΝ TUE WEDFRITHUSAT SUNa3-methylpentane is for colourless liquidTIMEcharacteristic smell that reactswith awith brominelegried (a diatomiccatalyst,asonemolecule) in the presence of3-methylpentane riquidA bromo 3-mformed through thecompoundhydrogen with brom:Subsitution of one->wrike a balance equation for thisreaction and explain of it requiresgasgaBalancingIt drogen bromide gove abonalso a product of this rensence of cabaystwokeO SEARCHplololololouldyou exp во свth + mars11boyour17https://learn2.open.ac.uk/mod/oucceerrrrrrrromineche

The initial reactants for the given reaction are- 3-methylpentane, Bromine liquid. The final…

a 3-methylpentare is FRE with a the ine characteristic smell that reacts with bromine leguied (a diatomic molecule) in the presence of a catalyst, A bromo 3-methylpentane riquid compound is formed through Subsitution of one hydrogen with & this ->write a balance equation for reaction and explain of it requires 5 I drogen bromide gavearbon of cabayst abo a product of the prensen Aontain woke

a 3-methylpentare is FRE with a the ine characteristic smell that reacts with bromine leguied (a diatomic molecule) in the presence of a catalyst, A bromo 3-methylpentane riquid compound is formed through Subsitution of one hydrogen with & this ->write a balance equation for reaction and explain of it requires 5 I drogen bromide gavearbon of cabayst abo a product of the prensen Aontain woke

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter27: Biomolecules: Lipids

Section27.SE: Something Extra

Problem 47AP: Cembrene, C20H32, is a diterpenoid hydrocarbon isolated from pine resin. Cembrene has a UV...

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Organotin compounds play a significant role in diverse industrial applications. They have been used as plastic stabilizers and as pesticides or fungicides.One method used to prepare simple tetraalkylstannanes is the controlled direct reaction of liquid tin(IV) chloride with highly reactive trialkylaluminum compounds, such as liquid triethylaluminum (Al(C2H5)3). 3SnCl4 + 4Al(C2H5)3 3Sn(C2H5)4 + 4AlCl3 In one experiment, 0.230 L of SnCl4 (d = 2.226 g/mL) was treated with 0.396 L of triethylaluminum (Al(C2H5)3); d = 0.835 g/mL). If 0.335 L of tetraethylstannane (d = 1.187 g/mL) were actually isolated in this experiment, what was the percent yield?
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