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prisoha [69]
4 years ago
12

The speed of a motorcycle increases from 10 kilometers per hour to 50 kilometers per hour in 9 seconds. What is its acceleration

?
Chemistry
1 answer:
Vesnalui [34]4 years ago
5 0

Answer:

well, it increased by 40 km/hr in 9 s, so the acceleration is

40/9 km/(hr-s)

Explanation:

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Which of the objects in the table has the most gravitational potential energy? Explain your answer.
Ganezh [65]

Answer:

Bowling Ball

Explanation:

The bowling ball has the highest gravitational potential energy because the height at which it will fall is the highest of the rest objects on the table.

8 0
2 years ago
If 155 grams of potassium (K) reacts with 122 grams of potassium nitrate (KNO3), what is the limiting reagent?
GenaCL600 [577]
K:

m=155g
M=39g/mol

n = 155g / 39g/mol ≈ 3,97mol

KNO₃:

m=122g
M=101g/mol

n = 122g/101g/mol = 1,21mol

2K          +            10KNO₃  ⇒  6K₂O + N₂
2mol        :            10mol
3,97mol   :           1,21mol
                             limiting reagent

KNO₃ is limiting reagent

5 0
3 years ago
X2o3 express you answer as a whole number
kobusy [5.1K]
 <span>2.40 - 1.68 =0.72 g of oxigen 
moles = 0.72/16 g/mol=0.045 

moles x = 1.68/ 55.9=0.03 

0.03/0.03 = 1 = x 
0.045 / 0.03 = 1.5 = O 

to get whole numbers multiply by 2 

x2O3 

X2O3 +3 CO = 2 X + 3 CO2</span>
4 0
4 years ago
What will determine the number of moles of hydronium in an aqueous solution of a strong monoprotic acid?.
marin [14]

Answer:

What will determine the number of moles of hydronium in an aqueous solution of a strong monoprotic acid? The amount of acid that was added.

Explanation:

3 0
2 years ago
Why do you require an acid catalyst to make an ester? Why not just mix acid and alcohol? Describe an alternate method of making
djverab [1.8K]

Answer:Acid catalyst is needed to increase the electrophilicity of Carbonyl group of Carboxylic acid as alcohol is a weak nucleophile.

Alternatively esters can be synthesised by converting carboxylic acid into acyl chloride using thionyl chloride(SOCl_{2} and then further treating acyl chloride with alcohol.

Carboxylic acid and esters can be easily distinguished on the basis of IR as carboxylic acid would contain a broad intense peak in 2500-3200cm_{-1} corresponding to OH stretching frequency whereas esters would not contain any such broad intense peak.

Alcohol and esters can also be distinguished using IR as alcohols would contain a broad intense peak at around 3200-3600cm_{-1}

Explanation: For the synthesis of esters using alcohol and carboxylic acid we need to add a little amount of acid in the reaction . The acid used here increases the electrophilicity of carbonyl carbon and hence makes it easier for a weaker nucleophile like alcohol to attack the carbonyl carbon of acid.

The oxygen of the carbonyl group is protonated using the acidic proton which  leads to the generation of positive charge on the oxygen. The positive charge generated is delocalised over the whole acid molecule and hence the electrophilicity of carbonyl group is increased. Kindly refer attachment for the structures.

If we simply mix the acid and alcohol then no appreciable reaction would take place between them and ester formation would not take place because the carboxylic acid in that case is not a good electrophile whereas alcohol is also not a very strong nucleophile which can attack the carbonyl group.

Alternatively we can use thionyl chloride or any other reagent which can convert the carboxylic acid into acyl chloride. Acyl chloride is very elctrophilic and alcohol can very easily attack the acyl chloride and esters could be synthesized.

The carboxylic acid and ester can very easily be distinguished on the basis of broad intense OH stretching frequency peak at around 2500-3200cm_{-1} . The broad intense OH stretching frequency peak is present in carboxylic acids as they contain OH groups and absent in case of esters .

Likewise esters and alcohols can also be distinguished on the basis IR spectra as alcohols will have broad intense spectra  at around 3200-3600cm_{-1}corresponding to OH stretching frequency whereas esters will not have any such peak. Rather esters would be having a Carbonyl stretching frequency at around 1720-1760

4 0
3 years ago
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