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andrey2020 [161]
3 years ago
13

Need help with question 1 a b and c also question 3 ASAP help needed

Chemistry
1 answer:
Mariulka [41]3 years ago
5 0
What grade are you in because im in eighth grade and that is hard
i cant even look up the answer online

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Most of earths fresh water is in glaciers <br><br> True or false <br><br> PEASE HELPP
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Answer:

True

Explanation:

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Use the idea of diffuseition to explain how the smell of perfume travel​
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When perfume is sprayed in a room the particles of perfume diffuse with the particles in the air.
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A stream of negatively charged particles is called:
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Cathode rays are a stream of negatively charged particles or electrons in vacuum tubes. They were first seen by Johann Hittorf in 1869. They are named since they are emitted by electrode or cathode. In order to release the electrons, the electrons should first be detached from the atoms of the cathode.
4 0
4 years ago
A stone is dropped from the roof of a building; 2.00s after that, a second stone is thrown straight down with an initial speed o
Brut [27]
A) -0.5(9.8)*t^2 = -25(t-2) - 0.5(9.8)(t-2)^2 
-4.9t^2 = -25t + 50 - 4.9(t^2-4t+4) 
0 = -25t+50+19.6t - 19.6 
5.4t = 30.4 
t = 5.62962963 s 

b) h = -4.9(5.62962963)^2 
h = -155.2943759 
the building is 155.2943759 m high 

c) speed 0of first stone 
= at 
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speed of second stone
= v + at
= 25+9.8*3.62962963 
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7 0
4 years ago
What is the major organic product obtained from the following reaction?
trapecia [35]

The correct option is (b)

NaNH2 is an effective base. It can be a good nucleophile in the few situations where its strong basicity does not have negative side effects. It is employed in elimination reactions as well as the deprotonation of weak acids.Alkynes, alcohols, and a variety of other functional groups with acidic protons, such as esters and ketones, will all be deprotonated by NaNH2, a powerful base.Alkynes are deprotonated with NaNH2 to produce what are known as "acetylide" ions. These ions are powerful nucleophiles that can react with alkyl halides to create carbon-carbon bonds and add to carbonyls in an addition reaction.Acid/base and nucleophilic substitution are the two types of reactions.Using the right base, terminal alkynes can be deprotonated to produce a carbanion.A good C is the acetylide carbanion.The acetylide carbanion can undergo nucleophilic substitution reactions because it is a potent C nucleophile. (often SN2) with 1 or 2 alkyl halides with electrophilic C to create an internal alkyne (Cl, Br, or I).Elimination is more likely to occur with 3-alkyl halides.It is possible to swap either one or both of the terminal H atoms in ethylene (acetylene) to create monosubstituted (R-C-C-H) and symmetrical (R = R') or unsymmetrical (R not equal to R') disubstituted alkynes (R-C-C-R').

Learn more about NANH2 here :-

brainly.com/question/12601787

#SPJ4

7 0
2 years ago
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