How much energy is required to boil 65 grams of 100°C water And then heat the steam to 150°C?

Chemistry

1 answer:

Artyom0805 [142]2 years ago

8 0

Answer:

13598 J

Explanation:

Q = m × c × ∆T

Where;

Q = amount of energy (J)

m = mass (grams)

c = specific heat capacity

∆T = change in temperature

m = 65g, specific heat capacity of water = 4.184J/g°C, initial temperature= 100°C, final temperature = 150°C

Q = 65 × 4.184 × (150 - 100)

Q = 271.96 × 50

Q = 13598 J

Hence, 13598 J of energy is required to boil 65 grams of 100°C water and then heat the steam to 150°C.

You might be interested in

8moles of Na2Cr2O2 is how much mass

Margaret [11]

$\boxed{\boxed{\mathfrak{ 1\: mole \:of \:Na_2Cr_2O_2\: = \:it's \:Gram\: Mol. \: mass}} }$

$\underline{ \mathfrak{ Gram \:molecular \:mass \:of \: \red{ Na_2Cr_2O_2}}}$

= 2 × 23 + 2 × 52 + 2 × 16

= 182 grams

1 mole of $Na_2Cr_2O_2$ weighs = 182 g

8 moles weigh = 8× 182

= $\mathfrak{\blue {\boxed{\underline {1456 \: grams}}}}$

$\mathfrak{\blue {\boxed{\underline {1. 46 \:kg }}}}$

5 0

2 years ago

Explain why the Amazon River does not create deltas?

jeka57 [31]

Answer:

The ocean currents are too strong by the Amazon River to form deltas.

Explanation:

The Atlantic has sufficient wave and tidal energy to carry most of the Amazon's sediments out to sea, thus the Amazon does not form a true delta. The great deltas of the world are all in relatively protected bodies of water, while the Amazon empties directly into the turbulent Atlantic.

4 0

1 year ago

When methyloxirane is treated with HBr, the bromide ion attacks the less substituted position. However, when phenyloxirane is tr

konstantin123 [22]

Answer:

See explanation and picture below

Explanation:

First, in the case of methyloxirane (Also known as propilene oxide) the mechanism that is taking place there is something similar to a Sn2 mechanism. Although a Sn2 mechanism is a bimolecular substitution taking place in only step, the mechanism followed here is pretty similar after the first step.

In both cases, the H atom of the HBr goes to the oxygen in the molecule. You'll have a OH⁺ in both. However, in the case of methyloxirane the next step is a Sn2 mechanism step, the bromide ion will go to the less substitued carbon, because the methyl group is exerting a steric hindrance. Not a big one but it has a little effect there, that's why the bromide will rather go to the carbon with more hydrogens. and the final product is formed.

In the case of phenyloxirane, once the OH⁺ is formed, the next step is a Sn1 mechanism. In this case, the bond C - OH⁺ is opened on the side of the phenyl to stabilize the OH. This is because that carbon is more stable than the carbon with no phenyl. (A 3° carbon is more stable than a 2° carbon). Therefore, when this bond opens, the bromide will go there in the next step, and the final product is formed. See picture below for mechanism and products.