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sesenic [268]
3 years ago
8

Which statement about technology is true?

Chemistry
2 answers:
photoshop1234 [79]3 years ago
8 0

Answer:

Technology improves a scientist's ability to make observations.

Explanation:

11Alexandr11 [23.1K]3 years ago
6 0

Answer:

Technology improves a scientist's ability to make observations.

Explanation:

You might be interested in
What ingredients are needed to turn the cake mix into cake batter​
svp [43]

Answer:

Ingredients

2 ⅓ cups all-purpose flour.

1 tablespoon baking powder.

¾ teaspoon salt.

1 ½ cups white sugar.

½ cup shortening.

2 eggs.

1 cup milk.

1 teaspoon vanilla extract.

Explanation:

4 0
3 years ago
Consider the pka (3.75) of formic acid, h-cooh as a reference. with appropriate examples, show how inductive, dipole, and resona
Luden [163]
Formic acid is the simplest carboxylic acid with a structure of HCOOH and has a pka of 3.75. The pka refers to the acidity of the molecule, which in this example refers to the molecules ability to give up the proton of the O-H. A decrease in the pka value corresponds to an increase in acidity, or an increase in the ability to give up a proton. When an acid gives up a proton, the remaining anionic species (in this case HCOO-) is called the conjugate base, and an increase in the stability of the conjugate base corresponds to an increase in acidity.

The pka of a carboxylic can be affected greatly by the presence of various functional groups within its structure. An example of an inductive effect changing the pka can be shown with trichloroacetic acid, Cl3CCOOH. This molecule has a pka of 0.7. The decrease in pka relative to formic acid is due to the presence of the Cl3C- group, and more specifically the presence of the chlorine atoms. The electronegative chlorine atoms are able to withdraw the electron density away from the oxygen atoms and towards themselves, thus helping to stabilize the negative charge and stabilize the conjugate base. This results in an increase in acidity and decrease in pka.

The same Cl3CCOOH example can be used to explain how dipoles can effect the acidity of carboxylic acids. Compared to standard acetic acid, H3CCOOH with a pka of 4.76, trichloroacetic acid is much more acidic. The difference between these structures is the presence of C-Cl bonds in place of C-H bonds. A C-Cl bond is much more polar than a C-H bond, due the large electronegativity of the chlorine atom. This results in a carbon with a partial positive charge and a chlorine with a partial negative charge. In the conjugate base of the acid, where the molecule has a negative charge localized on the oxygen atoms, the dipole moment of the C-Cl bond is oriented such that the partial positive charge is on the carbon that is adjacent to the oxygen atoms containing the negative charge. Therefore, the electrostatic attraction between the positive end of the C-Cl dipole and the negative charge of the anionic oxygen helps to stabilize the entire species. This level of stabilization is not present in acetic acid where there are C-H bonds instead of C-Cl bonds since the C-H bonds do not have a large dipole moment.

To understand how resonance can affect the pka of a species, we can simply compare the pka of a simple alcohol such as methanol, CH3OH, and formic acid, HCOOH. The pka of methanol is 16, suggesting that is is a very weak acid. Once methanol gives up that proton to become the conjugate base CH3O-, the charge cannot be stabilized in any way and is simply localized on the oxygen atom. However, with a carboxylic acid, the conjugate base, HCOO-, can stabilize the negative charge. The lone pair electrons containing the charge on the oxygen atom are able to migrate to the other oxygen atom of the carboxylic acid. The negative charge can now be shared between the two electronegative oxygen atoms, thus stabilizing the charge and decreasing the pka.
3 0
4 years ago
The specific spatial arrangement of amino acid residues that are close to each other in the polypeptide chain is called______the
natulia [17]

Answer:

c. tertiary.

Explanation:

In this case, we can review the definition of each level of structuration in the proteins:

<u>Primary structure</u>

<u />

In the primary structure, the amino acids are linked by peptide bonds. That is, the order of the amino acids is the criterion that defines this type of structure.

<u>Secondary structure</u>

<u />

In the secondary structure, we have to look at the way in which the protein is folded. The options are:

  -) Beta-laminar: A structure in which the protein has a planar shape.

  -) Alpha-helix: A structure in which the protein has a cross-strand form.

<u>Tertiary structure</u>

<u />

In the tertiary structure, the R groups that the amino acids have in the primary structure can generate interactions with each other. Interactions such as hydrogen bridges, dipole-dipole, hydrophobic interactions. This makes the protein have a very specific three-dimensional structure, on which its function depends.

<u>Quaternary structure</u>

<u />

In the quaternary structure, several subunits may be attached, or there may be prostatic groups (metals that can help to attach various protein units).

With all these in mind, the deffinition that fits with the description in the question is the <u>tertiary structure.</u>

I hope it helps!

<u />

4 0
3 years ago
Does this sound catchy or invite you to read more? "GMOs and pesticides are general amongst farmers for generations and should n
siniylev [52]

Answer:

It sounds fine, but it may be a bit too long. It's difficult to shorten things like this, but getting more straight to the point would give it that "catchy" feel.

Explanation:

3 0
3 years ago
SOME ONE HELP I FORGOT PIC!!! 20 POINTS AND BRAINLIEST!!!
stiks02 [169]

spindle fibers

i think the next is two nuclei and still together but that stage is not anaphase. Anaphase is when the sister chromatids are pulled apart

8 0
3 years ago
Read 2 more answers
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