hi friend the earth spin at 1,000 in meters per hour
I hope it helped you
Answer:
For object A
m = 5 kg , v= -11 j
For B object
m = 6 kg , v= 5 i +8.7 j
For object C
m = 10 kg , v= -10 i
We know that
Linear momentum P= m v kg.m/s
a) A and C
Momentum in y direction
Py=- 5 x 11 j= - 55 j kg.m/s
Momentum in x direction
Px=- 10 x 10 j= - 100 i kg.m/s
b) B and C
Momentum in y direction
Py=6 x 8.7 j= 52.2 j kg.m/s
Momentum in x direction
Px=( 6 x 5 - 10 x 10 ) i = - 70 i kg.m/s
c) A ,B and C
By using data of a and b
Momentum in y direction
Py= 6 x 8.7 - 5 x 11 j= -2.8 j kg.m/s
Momentum in x direction
Px= 6 x 5 -10 x 10 i = -70 i kg.m/s
<h2>
Answer:</h2>
C.
<h2>
Explanation:</h2>
This is what we call a permanent magnet. By the way, the magnetic phenomena were first observed about 2500 years ago near the ancient city of Magnesia, what is today Manisa, located in western Turkey, when people saw fragments of magnetized iron. So <em>what happens if you cut a magnet in half? </em>Well, a magnet has two ends, the first one is called a north pole or N pole while the other end is a south pole or S pole, so if you break a bar magnet, each piece has a north and south pole, no matter the size of each new bar although the smaller the piece, the weaker its magnetism. This is true because unlike electric charges, you always find magnetic poles in pairs, that is, ¡they can't be isolated! The option is C. because in the great bar the north pole is to the left while the south pole is to right.
Answer:
Sagittarius
Explanation:
The center of the Milky Way galaxy lies in the direction of the Sagittarius constellation, about 26,000 light-years away.
Answer:
Explanation:
The equilibrium mechanism for the reversible acid is catalyzed by the isomerization of non conjugated β, γ- unsaturated ketones, like 3-cyclohexanone to their conjugated α, I²- unsaturated isomers.
Oxygen of the Carbonyl group in the ketone is protonated by the acid and this is followed by the abstraction of an α- hydrogen from the protonated 3-cyclo hexanone to yield ethanol
2-cyclo hexanone can be obtained by acid catalyzation of 3-cyclohexanone isomers through the formation of it's "enol".
