Chemistry College

What is one way a pathogen can enter the body?

Question 3 options:

Nose


Broken Skin


Mouth


All of the above

Answers

Answer 1
I’m pretty sure it’s Nose
Answer 2
Answer: All of the above

Explanation: Microorganisms capable of causing disease—pathogens—usually enter our bodies through the mouth, eyes, nose, or urogenital openings, or through wounds or bites that breach the skin barrier.

I hope this helped! Please mark this answer as brainliest if you don’t mind <3

Related Questions

Please help me ASAP I’ll mark Brainly

Answers

Answer:

Batteries hold chemical energy

Explanation:

The battery acid in a battery leads to chemical energy.

The density of gold is 19.3 g/cm³. Which of the following shows the mass of a gold bar that is 4.50 cm × 8.00 cm × 20.00 cm?

Answers

Answer:

13896g

Explanation:

volume = 4.50×8.00×20.00 = 720 cm³

mass = density × volume

mass= 19.3 × 720 = 13896g

Identify the most acidic hydrogens in each of the following molecules. Give the structure of the enolate ion arising from deprotonation. (a) Acetaldehyde; (b) propanal; (c) acetone; (d) 4-heptanone; (e) cyclopentanone.

Answers

Answer:

See explanation below (Brainlist please)

Explanation:

First of all, we need to understand what is an acidic hydrogen.

An acidic hydrogen, is the atom of hydrogen which is more propense to undergo an acid base reaction, and form a stable ion or molecule in the process.

In other words, is the hydrogen that is more vulnerable to get substracted in an acid base reaction to form another compound.

Knowing this information, gives us an idea of how a molecule can be formed and which kind of compound is formed.

Now, in this question, we have 5 molecules. Each of them is either a ketone or aldehyde, so this mean that we have the carbonile group (C = O), which means that is easier to identify the acidic hydrogen. This is because the Carbonile group is an attractor group, so, it will attract the charges by inductive effect (in some cases by resonance), and the molecule is more stable.

This can be shown by drawing the enolate ion that is formed once the molecule undergo the acid base reaction. As it's an enolate form that we are looking for, then it means that the ketone or aldehyde is undergoing an electrofilic attack with a base. This base will substract the most acidic hydrogen to form a better and stable enolate. The acidic hydrogen and the enolate form can be seen in the attached picture.

a) In the case of acetaldehyde, the most acidic will be the hydrogen of carbon 2, because the hydrogen from the carbonile, once it's substracted, the charge of the carbon cannot be stabilized by resonance. Carbon 2 hydrogens, can do this job easily.

b) Propanal happens something similar to acetaldehyde, the terminal hydrogen cannot be substracted, and carbon 3, once the hydrogen is gone, the negative charge cannot be stabilized by resonance, so hydrogens of carbon 2 can do this.

c) in the case of acetone, is easier to look because we only have the C = O between two methyl group, so you can use either carbon 1 or 3 to do the job.

d) 4 heptanone the most acidic hydrogen would be carbon 3 or 5, because they are closer to the C=O and the ion can be stabilized by resonance.

e) Finally in ciclopentanone, the most acidic hydrogen would be carbon 2 or 5.

See picture for a better understanding.

Hope it helps.

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