Answer:
Physical and psychological dependence is high, and withdrawal symptoms include watery eyes, runny nose, loss of appetite, irritability, tremors, panic, abdominal cramps and diarrhea, nausea, chills, and sweating. Use of contaminated syringes/needles to inject drugs may result in serious blood borne infections such as HIV-AIDS and hepatitis.
Answer:
Well they didn't transfer any energy when they weren’t touching and it did t produce any energy if it didn’t move. Since they are on top of each other they are causing momentum on each other creating kinetic energy
Explanation:
The statement is true in this situation is C. The size of Ffric is the same as the size of Fapp:
From the diagram, since the body is in equilibrium, the sum of vertical forces equals zero. Also, the sum of horizontal forces equal zero.
So, ∑Fx = 0 and ∑Fy = 0
Since Fapp acts in the negative x - direction and Ffric acts in the positive x - direction,
∑Fx = -Fapp + Ffric = 0
-Fapp + Ffric = 0
Fapp = Ffric
Also, since Fgrav acts in the negative y - direction and Fnorm acts in the positive y - direction,
∑Fy = Fnorm + (-Fgrav) = 0
Fnorm - Fgrav = 0
Fnorm = Fgrav
So, we see that the size of Fapp <u>equals</u> size of Ffric and the size of Fnorm <u>equals</u> the size of Fgrav.
So, the correct option is C
The statement which is true in this situation is C. The size of Ffric is the same as the size of Fapp.
Learn more about equilibrium of forces here:
brainly.com/question/12980489
Answer:
B Genes determine specific traits while the chromosomes contain these genes
Answer and explanation:
cyclopentadiene is more acidic than cyclopentane
hydrocarbon compound are weak acid in nature
This relative acidity is explained by the stability of
cyclopentadienyl anion which is aromatic in nature
(check the attached image file 1)
To answer this question we must look at the stability of the anions that are formed when the compound lose proton.
All the electron in the cyclopentyl anion are localized.
In contrast, the aromatic cyclopentadienyl anion is a stable carbanion as a result of its aromaticity therefore making its conjugate acid a very strong acid compare to other compounds with hydrogen attached to sp³ carbons
