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kramer
3 years ago
13

Which molecule is polar, based on structure? 1) sulfur dioxide 2) carbon disulphide 3) ethylene 4) carbon tetrachloride

Chemistry
2 answers:
alexandr402 [8]3 years ago
7 0

The answer is 1) sulfur dioxide.

Savatey [412]3 years ago
4 0
I think the correct answer from the choices listed above is option 1. It would be the molecule carbon disulphide that will be polar, based on the structure of the choices given. Hope this answers the question. Have a nice day. Feel free to ask more questions.
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Deep sea divers can experience the bends due to an increased amount of nitrogen in the blood
garri49 [273]

b is the correct answer

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3 years ago
How does it? Please help
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3 years ago
Rasheed calculates that his chemical reaction should produce 4 moles of product, but when he does the experiment, he gets only 3
Brut [27]

Answer:

The answer to your question is 75%

Explanation:

Data

Theoretical production = 4 moles

Experimental production = 3 moles

Percent yield = ?

Formula

Percent yield = \frac{Experimental production}{Theoretical production} x 100

Substitution

Percent yield = \frac{3}{4} x 100

Result

Percent yield = 75 %

8 0
3 years ago
What type of covalent bond is formed between amino acid molecules during protein synthesis? peptide bond electrovalent bond hydr
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The type of covalent bond is formed between amino acid molecules during protein synthesis will be  <u>"peptide bond".</u>

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A peptide bond would be a sort of covalent link that connects an amino acid's carboxyl group to its amino group. Amino acids itself were comprised of atoms bonded together through covalent bonds.

Two atoms share an electron pair equally in a covalent link. Peptide (amide) but also disulfide links between amino acids, as well as C-C, C-O, and C-N bonds within amino acids, represent examples of significant covalent bonds.

Therefore, the type of covalent bond is formed between amino acid molecules during protein synthesis will be  <u>"</u><u>peptide bond"</u><u>.</u>

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8 0
1 year ago
Which 2 resonance forms destablize the carbocation intermediate if bezonitrile undergoes chlronation at the ortho or para positi
Anna11 [10]

The question is incomplete, the complete question is shown in the image attached

Answer:

A and B

Explanation:

The electrophilic substitution of arenes yields a cation intermediate. The positive charge of the cation is delocalized over the entire ring.

The -CN group directs incoming electrophiles to the ortho/para position. The resonance structures for the chlorination of benzonitrile are shown in the question.

Recall that -CN is an electron withdrawing group. The resonance forms that destablize the carbocation intermediate are those in which the -CN group is directly attached to the carbon atom bearing the positive charge as in structures A and B.

8 0
3 years ago
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