A car starts from rest and after 20 seconds it's velocity becomes 108km find the acceleration of the car

Physics

1 answer:

andre [41]3 years ago

7 0

Answer:

1.5 km/s²

Explanation:

Given that:

a car starts from rest; it means the initial velocity (u) = 0 km/hr = 0 m/s

after time (t) = 20 seconds

the final velocity = 108 km/hr = 30 m/s

The acceleration (a) of the car can be determined by using the formula:

$a = \dfrac{v-u}{t}$

$a = \dfrac{30\ m/s -0 \ m/s}{20 \ s}$

$a = \dfrac{30 \ m/s}{20 \ s}$

a = 1.5 km/s²

You might be interested in

The thunderbolt bobsled team is training for Olympic Gold. During practice they start a run with a speed of 0.57 m/s, they compl

aleksandr82 [10.1K]

$acceleration=\frac{\Delta\ velocity}{\Delta\ time}\\\\
v_{initial}=0,57m/s\\
distance=1360m\\ \Delta\ time=89,49seconds\\\\
v_{final}-v_{initial}=\frac{distance}{time}\\
v_{final}=\frac{distance}{time}+v_{initial}\\
v_{final}=\frac{1360}{89,49}+0,57\\\\v_{final}=15,77\frac{m}{s}\\\\
acceleration=\frac{15,77-0,57}{89,49}=0,17\frac{m}{s^2}\\\\ \boxed{acceleration=0,17\frac{m}{s^2}}$

6 0

3 years ago

Give the relationship(s) for any pair of protons with the proper term(s). Label – your choice. A.Heterotopic B.Heterotopic, dias

Afina-wow [57]

Answer and Explanation

• Heterotopic protons are those that when substituted by the same substituent, are structurally different. They are not similar, diastereotopic or enantiotopic.

• Diastreotopic protons refers to two protons in a molecule which, if replaced by the same substituent, would generate compounds that are diastereomers. Diastereotopic groups are often, but not always, identical groups attached to the same atom in a molecule containing at least one chiral center.

For example, the two hydrogen atoms of the C3 carbon in (S)-2-bromobutane are diastereotopic (shown in the attached image). Replacement of one hydrogen atom with a bromine atom will produce (2S,3R)-2,3-dibromobutane. Replacement of the other hydrogen atom with a bromine atom will produce the diastereomer (2S,3S)-2,3-dibromobutane.

• Homotopic protons in a compound are equivalent protons. Two protons A and B are homotopic if the molecule remains the same (including stereochemically) when the protons are interchanged with some other atom (substituent) while the remaining parts of the molecule stay fixed. Homotopic atoms are always identical, in any environment.

For example, ethane, the two H atoms on C1 and C2 carbons on the same side (as shown in the attached image) are homotopic as they exhibit the phenomenon described above.

• Enantiotopic protons are two protons in a molecule which, if one or the other were replaced (by the same substituent), would generate a chiral compound. The two possible compounds resulting from that replacement would be enantiomers.

For example, in the attached image to this answer, the two hydrogen atoms attached to the second carbon in butane are enantiotopic. Replacement of one hydrogen atom with a bromine atom will produce (R)-2-bromobutane. Replacement of the other hydrogen atom with a bromine atom will produce the enantiomer (S)-2-bromobutane.

Hope this helps!!!