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Sati [7]
3 years ago
10

Please help fast I will give brainliest if correct

Chemistry
2 answers:
Leokris [45]3 years ago
8 0

Answer:

the answer you marked is correct

Iteru [2.4K]3 years ago
6 0

Answer:

the answer you marked is correct

Explanation:

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B

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They lose energy and slow down and move closer to other gas molecules and the molecules collect together to form a liquid

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Which property of gases best explains the ability of air bags to cushion the force of impact during a car accident?
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Gases are compressible
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Which compound contains both sigma and pi bonds? HCCl3 H2CO H2S HBr.
Aliun [14]

The compound that contains both sigma and pi bonds has been \rm \bold{H_2CO}. Thus, option B is correct.

The compounds have been resulted by the sharing of the valence electrons between atoms, for the completion of octet of each elements.

The bonds can be saturated with the presence of only sigma bond. The unsaturated bonds has presence of pi bonds as well. The bond with one pi and one sigma has been a double bond, while 1 sigma and 2 pi has been a triple bond.

The bonds present in the following structures has been:

\rm HCCl_3=4\;\sigma\;bonds\\H_2CO=2\;\sigma,\;1\;\pi\;bond\\H_2S=2\;\sigma\;bonds\\HBr\;=1\;\sigma\;bond

The compound with the presence of both sigma and pi bonds has been \rm \bold{H_2CO}. Thus, option B is correct.

For more information about the sigma and pi bonds, refer to the link:

brainly.com/question/14018074

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2 years ago
Which of the following is NOT a function of the skeletal system?
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production od blood cells

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3 years ago
each of the following reactions has been reported in the chemical literature. predict the product in each case, showing stereoch
poizon [28]

(a): This is an elimination reaction. The reaction proceeds in 3 steps; Step 1: Protonation of alcohol, step 2: Loss of leaving group, and step 3: Deprotonation to form an alkene. Elimination (E1) reaction dominates than substitution (SN1) reaction because the formed HSO4- anion is a poor nucleophile and tends not to add to the carbocation intermediate formed. Hence the product formed is I, is trans.

(b) This is a dihydroxylation of the alkenes reaction. A catalytic amount of OsO4 is used along with an oxidizing agent, which oxidizes the reduced osmium(VI) into osmium(VIII) to regenerate the catalyst. The reaction proceeds in 2 steps; Step 1: Cis addition of OsO4 to double bond and form 4 member cyclic osmate ester. Step 2: Hydrolysis of the intermediate to 1.2-diol. Hence the product formed is II, is cis. 

(c) This is hydroboration - oxidation reaction. The reaction proceeds through the addition of H- on the more substituted carbon and BH2 on the less substituted carbon of the double bond. The reaction is a syn addition. Hence the product formed is III.

(d) This a reduction reaction where carboxylic acid (-COOH) is reduced to 1o alcohol (-CH2OH). Hence the formed product is IV.

Stereochemistry, a subdiscipline of chemistry, involves the take a look at the relative spatial association of atoms that form the shape of molecules and their manipulation.

The observation of stereochemistry specializes in stereoisomers, which by means of definition have an equal molecular method and series of bonded atoms (constitution), however, differ within the three-dimensional orientations of their atoms in space. for that reason, it's also referred to as 3-d chemistry three-dimensionality.

Learn more about  Stereochemistry here:-brainly.com/question/13266152

#SPJ4

<u>Disclaimer:- your question is incomplete, please see below for the complete question.</u>

Each of the following reactions has been reported in the chemical literature. Predict the product in each case, showing stereochemistry where appropriate.

5 0
1 year ago
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