Here we have to draw the four isomers of the compound 3-bromo-4-fluorohexane.
The four isomers of the compound is shown in the figure.
In an organic molecule the chiral -C center is that where four (4) different groups are present. In 3-bromo-4-fluorohexane the 3 and 4 positions are chiral centers. The possible isomers of a molecule can be obtained from the formula 2n. As here 2 chiral centers are present thus number of stereoisomers will be 2×2 = 4.
The four different isomers as shown in the figure are 3R-, 4R-; 3S-, 4S; 3R, 4S and 3S-, 4R- 3-bromo-4-fluorohexane.
In the 3-bromo-4-fluorohexane the functional groups are -Br, C₂H₅, -C₃H₆F and -H for 3-position and -F, -C₂H₅, -C₃H₆ and -H for 4-position respectively.
The priority of the -3 position will be Br > C₃H₆F > C₂H₅ > H and for -4 position F > C₃H₆Br > C₂H₅ > H. If the rotation from the higher priority group to lower is clockwise and anticlockwise then the S- and R- notation are used respectively. However if the -H atom is present at the horizontal position then the notation will be reverse.
Thus the four isomers of the compound is shown.
Answer:
643g of methane will there be in the room
Explanation:
To solve this question we must, as first, find the volume of methane after 1h = 3600s. With the volume we can find the moles of methane using PV = nRT -<em>Assuming STP-</em>. With the moles and the molar mass of methane (16g/mol) we can find the mass of methane gas after 1 hour as follows:
<em>Volume Methane:</em>
3600s * (0.25L / s) = 900L Methane
<em>Moles methane:</em>
PV = nRT; PV / RT = n
<em>Where P = 1atm at STP, V is volume = 900L; R is gas constant = 0.082atmL/molK; T is absolute temperature = 273.15K at sTP</em>
Replacing:
PV / RT = n
1atm*900L / 0.082atmL/molK*273.15 = n
n = 40.18mol methane
<em>Mass methane:</em>
40.18 moles * (16g/mol) =
<h3>643g of methane will there be in the room</h3>
In order to deprotonate an acid, we must remove protons in order to achieve a more stable conjugate base. For this example, we can use the relationship between carboxylic acid and hydroxide.
Deprotonation is the removal of a proton from a specific type of acid in reaction to its coming into contact with a strong base. The compound formed from this reaction is known as the conjugate base of that acid. The opposite process is also possible and is when a proton is added to a special kind of base. This is a process referred to as protonation, which forms the conjugate acid of that base.
For the example we have chosen to give, the conjugate base is the carboxylate salt. This would be the compound formed by the deprotonated carboxylic acid. The base in question was strong enough to deprotonate the acid due to the greater stability offered as a conjugated base.
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Answer: B: the reaction of gasoline combustion in the engine
Explanation:
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