Answer:
(D)9 divided by sin 60 degrees
Step-by-step explanation:
From the given figure, using trigonometry
Substituting the given values, we get
Thus, The length of the support AB is 9 divided by sin 60 degrees.
Answer:The crystal structures of five 6-mercaptopurine derivatives, viz. 2-[(9-acetyl-9H-purin-6-yl)sulfanyl]-1-(3-methoxyphenyl)ethan-1-one (1), C16H14N4O3S, 2-[(9-acetyl-9H-purin-6-yl)sulfanyl]-1-(4-methoxyphenyl)ethan-1-one (2), C16H14N4O3S, 2-[(9-acetyl-9H-purin-6-yl)sulfanyl]-1-(4-chlorophenyl)ethan-1-one (3), C15H11ClN4O2S, 2-[(9-acetyl-9H-purin-6-yl)sulfanyl]-1-(4-bromophenyl)ethan-1-one (4), C15H11BrN4O2S, and 1-(3-methoxyphenyl)-2-[(9H-purin-6-yl)sulfanyl]ethan-1-one (5), C14H12N4O2S. Compounds (2), (3) and (4) are isomorphous and accordingly their molecular and supramolecular structures are similar. An analysis of the dihedral angles between the purine and exocyclic phenyl rings show that the molecules of (1) and (5) are essentially planar but that in the case of the three isomorphous compounds (2), (3) and (4), these rings are twisted by a dihedral angle of approximately 38°. With the exception of (1) all molecules are linked by weak C—H⋯O hydrogen bonds in their crystals. There is π–π stacking in all compounds. A Cambridge Structural Database search revealed the existence of 11 deposited compounds containing the 1-phenyl-2-sulfanylethanone scaffold; of these, only eight have a cyclic ring as substituent, the majority of these being heterocycles.
Keywords: crystal structure, mercaptopurines, supramolecular structure
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Chemical context
Purines, purine nucleosides and their analogs, are nitrogen-containing heterocycles ubiquitous in nature and present in biological systems like man, plants and marine organisms (Legraverend, 2008 ▸). These types of heterocycles take part of the core structure of guanine and adenine in nucleic acids (DNA and RNA) being involved in diverse in vivo catabolic and anabolic metabolic pathways.
6-Mercaptopurine is a water insoluble purine analogue, which attracted attention due to its antitumor and immunosuppressive properties. The drug is used, among others, in the treatment of rheumathologic disorders, cancer and prevent
Step-by-step explanation:
-12 + 4 3/5 = -7.4 <--- decimal.
-6 2/7 + 3 1/14 = 3 3/14 <--- repeating decimal.
-2 2/3 + -3 3/4 = -6 5/12 <--- repeating decimal.
°.✩┈┈┈┈∘*┈┈୨♡୧┈┈*∘┈┈┈┈✩.°
I hope this helps you. It kind of helps me because, I wanna scream and cry and just stay in one room. So imma go outside and sit down.. and walk back to my room and scream into a pillow (っ◞‸◟c)
Answer:
x=1
Step-by-step explanation:
This stuff is quite easy in reality. Here's a little example including your numbers.
by this point we are left with simplifying it. Since it's a double negative we get a positive. Thus x=1
Answer:
The graph has a domain of all real numbers.
The graph has a y-intercept at 
.
The graph has an x-intercept at 
.
Step-by-step explanation:
Given: The graph is ![y=\sqrt[3]{x-1}+2](https://tex.z-dn.net/?f=y%3D%5Csqrt%5B3%5D%7Bx-1%7D%2B2)
The domain of a function is a set of input values for which the function is real and defined.
Thus, the graph has a domain of 
.
To find the y-intercept: To find the y-intercept, substitute 
in .
![\begin{aligned}y &=\sqrt[3]{x-1}+2 \\&=\sqrt[3]{0-1}+2 \\&=-1+2 \\&=1\end{aligned}](https://tex.z-dn.net/?f=%5Cbegin%7Baligned%7Dy%20%26%3D%5Csqrt%5B3%5D%7Bx-1%7D%2B2%20%5C%5C%26%3D%5Csqrt%5B3%5D%7B0-1%7D%2B2%20%5C%5C%26%3D-1%2B2%20%5C%5C%26%3D1%5Cend%7Baligned%7D)
Thus, the y-intercept is
To find the x-intercept: To find the x-intercept, substitute 
in .
![\begin{aligned}y &=\sqrt[3]{x-1}+2 \\0 &=\sqrt[3]{x-1}+2 \\-2 &=\sqrt[3]{x-1} \\(-2)^{3} &=(\sqrt[3]{x-1})^{3} \\-8 &=x-1 \\-7 &=x\end{aligned}](https://tex.z-dn.net/?f=%5Cbegin%7Baligned%7Dy%20%26%3D%5Csqrt%5B3%5D%7Bx-1%7D%2B2%20%5C%5C0%20%26%3D%5Csqrt%5B3%5D%7Bx-1%7D%2B2%20%5C%5C-2%20%26%3D%5Csqrt%5B3%5D%7Bx-1%7D%20%5C%5C%28-2%29%5E%7B3%7D%20%26%3D%28%5Csqrt%5B3%5D%7Bx-1%7D%29%5E%7B3%7D%20%5C%5C-8%20%26%3Dx-1%20%5C%5C-7%20%26%3Dx%5Cend%7Baligned%7D)
Thus, the x-intercept is
