Answer:The functional groups in an organic compound can frequently be deduced from its infrared absorption spectrum. A compound, C5H10O2, exhibits strong, broad absorption across the 2500-3200 cm^1 region and an intense absorption at 1715 cm'^-1. Relative absorption intensity: (s)=strong, (m)-medium, (w) weak. What functional class(cs) docs the compound belong to List only classes for which evidence is given here. Attach no significance to evidence not cited explicitly. Do not over-interpret exact absorption band positions. None of your inferences should depend on small differences like 10 to 20 cm^1. The functional class(es) of thla compound is(are) alkane (List only if no other functional class applies.) alkene terminal alkyne internal alkyne arene alcohol ether amine aldehyde or ketone carboxylic acid ester nitr
Petrol is a conductor of electricity, because it conducts rather than insulates.
The movement of the plates creates three types of tectonic boundaries: convergent, where plates move into one another; divergent, where plates move apart; and transform, where plates move sideways in relation to each other. Hope this helps! :D
Answer:
D. +5.7 kJ/mol
Explanation:
Molar free energy (ΔG) in the transportation of uncharged molecules as glucse through a cell membrane from the exterior to the interior of the cell is defined as:
ΔG = RT ln C in / C out
knowing R is 8,314472 kJ/molK; T is 298K Cin = 200mM and Cout = 20mM
ΔG = 5,7 kJ/mol
Right answer is:
D. +5.7 kJ/mol
I hope it helps!
Answer:
The correct answer is 4 substracting hydride ions from olefins.
Explanation:
The olefins are the unsaturated hydrocarbon also called alkenes that contain one double bond present between 2 carbon atoms.
On the other hand a carbenium ion is formed when a hydrocarbon loses a hydride ion to form a positively charged product.
For example allyl cation
CH2=CH-CH2+
The allyl cation is a carbenium ion formed by the removal of H- ion or hydride ion from the alkene propene.
