Answer:
The correct answer is <em>d. At equilibrium, the forward reaction and reverse reaction will have the same reaction rate.</em>
Explanation:
When a reaction begins, the reactants combine to form products. At the same time of product formation, the convertion of products into reactants also occur. The reaction reaches <em>chemical equilibrium </em>when the rate of forward reaction (the convertion of reactant into products) is equal to the rate of reverse reaction (the convertion of product into reactants). Upon this state, the concentration of reactants and products do not change in time (that does not mean that the concentration of reactants and products are equal, but that once the chemical equilibrium is reached, their concentrations at this point will not vary with the time because the forward and reverse reactions are occuring at the same velocity).
The information that should be added to the chart in order to find out who ran a greater distance is THE UNITS USED TO MEASURE DISTANCE EACH DAY.
In science, the use of units if very important and each record made must be accompany with relevant units that are appropriate for the measurement taken. If units are not used along with data, it will be very difficult to quantify the values that are recorded. Scientists all over the world use SI units in their works in order to ensure uniformity.
A petroleum-based lubricant used to in farming machinery.
hope i helped very well
Answer:
The stronger acid is HBrO3.
Explanation:
It has an additional oxygen making it more electronegative, in turn making it a stronger acid.
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.
