<span>3. All nucleotides are made up of three component compounds:
a 5-carbon sugar (ribose or deoxyribose),
a phosphate group, and
a nitrogenous base.</span>
Answer:
See explanation
Explanation:
Two structures are pictured in the image attached, structure 2 is a more stable structure for TeF₄ or TeCl₄ since the lone pair in the structure is present at an equatorial position. Note that the structure of the compound is based on a trigonal bipyramid but of the structure type AX4E, where the lone pair could be positioned at axial or equatorial positions as shown in the images attached.
As a result of repulsion between electron pairs, the bond distance between Te - X(axial) is greater than Te-X (equatorial). This implies that the Te - X(axial) bonds are longer than Te - X(equatorial) bonds.
In answering the question, we must take cognisance of the fact fluorine is more electronegative than chlorine. This implies that fluorine will draw more electron density towards itself than chlorine and this shortens the bond length.
The structures of the both compounds are based on a trigonal bipyramid with a bond angle of 90° for axial position and 120° for the equatorial position.
Owing to the greater electo negativity of fluorine, both the fluorine F-axial and F-equatorial bonds of TeF4 are shorter than the Cl-axial and Cl-equatorial bonds of TeCl4. Hence the axial and equatorial angles in TeF4 are smaller than the axial and equatorial bond angles in TeCl4 due to the greater electro negativity of the fluorine atom.
Answer:
What happened to the proton after absorbing an electron? It becomes neutral.
Explanation:
hope this helps
I am thinking the answer is B. I think this because Bohr had a model similar, but his was lacking the cloud of electrons. His just had electrons orbiting the nucleus.
I hope this is right!<span />
Answer:
See explanation and image attached
Explanation:
Aromatic compounds undergo electrophilic aromatic substitution reactions in which the aromatic ring is maintained.
Substituted benzenes may be more or less reactive towards electrophilic aromatic substitution than benzene depending on the nature of the substituent present in the ring.
Substituents that activate the ring towards electrophilic substitution such as -OCH3 are ortho-para directing.
The major products of the bromination of anisole are p-bromoanisole and o-bromoanisole. The resonance structures leading to these products are shown in the image attached.