In mixed form, it would be equal to 1 2/7
In short, Your Answer would be Option B
Hope this helps!
f<span>(x)</span>=<span>x^2</span>−<span>6
</span>Replace <span>f<span>(x)</span></span> with <span>yy</span>.
<span>y=<span>x^2</span>−<span>6
</span></span>Interchange the variables.
<span>x=<span>y2</span>−6
</span>Solve for <span>yy</span><span>.
</span>
Move <span><span>−6</span><span>-6</span></span> to the right side of the equation by subtracting <span><span>−6</span><span>-6</span></span> from both sides of the equation.<span><span><span>y2</span>=6+x</span><span><span>y2</span>=6+x</span></span>Take the <span><span>square</span><span>square</span></span> root of both sides of the <span><span>equation</span><span>equation</span></span> to eliminate the exponent on the left side.<span><span>y=±<span>√<span>6+x</span></span></span><span>y=±<span>6+x
</span></span></span>The complete solution is the result of both the positive and negative portions of the solution.
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<span>y=<span>√<span>6+x</span></span>,−<span>√<span>6+x</span></span></span>
Solve for y<span> and replace with </span><span><span>f^<span>−1</span></span><span>(x).
</span></span>
<span>Answer is f<span>−1</span></span><span>(x)</span>=<span>√<span>6+x</span></span>,−<span>√<span>6+<span>x</span></span></span>
Answer: x ≥ 5
Step-by-step explanation:
7 is increased by the product of a number and 3: 7 + 3x
Is at least 22: ≥ 22
Your equation is: 7 + 3x ≥ 22
subtract 7 from both sides
3x ≥ 15
divide both sides by 3
x ≥ 5
Answer:
The graph answer choices are needed to answer this question, otherwise no one can help you.
Step-by-step explanation:
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:
