Hey I’m just setting up my profile so I’ll say fast
Both
in the domestic and international guidelines tell that when two power-driven
vessels are crossing so as to contain risk of collision, the vessel which has
the other on her starboard side (the give-way vessel) must keep out of the way.
If
you are the give-way vessel, it is your responsibility to avoid a collision. Normally,
this means you must change speed or direction to cross behind the other vessel
which is the stand-on vessel.
At
evening, when you perceive a red light crossing right-to-left in front of you,
you need to change your course. But if you perceive a green light crossing from
left-to-right, you are the stand-on vessel, and should maintain course and
speed.
The leading situations of collision risk are meeting head-on, overtaking, and crossing. When one of two vessels is to keep out of the way (give-way vessel), the other, the stand-on vessel, must uphold course and speed.
64. 16x16 = 4 so 9x9 divided by 2 equals 7
Not sure what the given options are, but the answer is the horizontal component. This is given by Force x cos(angle), or Fcos(θ), where θ is the angle. In this case that would be 20cos(30) = 17.32N
Answer:
Electrophilic aromatic substitution involves a process in an atom that is attached to an aromatic system is replaced by a electrophile. Electrophile is an electron pair acceptor. In the first step of electrophilic aromatic substitution of aniline, aniline has 3 resonance structures.
Explanation:
Aniline undergo a two step electrophilic aromatic substitution. The first step yields both ortho and para groups while the last yield a meta group.
In the first step, the amino group of aniline are strong activating group and ortho/para directing by resonance. This amino groups donates their unshared electrons to the pi-system creating a negative charge on the ortho and para positions. These positions are most reactive towards an electron-poor electrophile.
In the second step, the electrophilic aromatic substitution on aniline proceeds quite slowly to give an unexpected high yield of meta product.