Answer:
Reference image attached
Explanation:
Please see the attached image.
Hi. 2fouls! :)
First convert the number from kilometer to miles:


Now to find the miles per minutes,divide the miles per hours by 60 (the amount of minutes in an hour.)


The car is travelling at a speed of 0.860766667 miles/minute.
Hope this helps.
-Benjamin
Answer:
C.Melt both cubes and look for a broader range of melting temperatures. The one that melts over a broader range of temperatures is the amorphous solid.
Explanation:
Amorphous solids is one that do not have a fixed melting points but melt over a wide range of temperature due to the irregular shape hence its name. Contrariwise crystalline solids, have a fixed and sharp melting point.
This comes in handy to solve the riddle. We can characterise the pair with the melting point property.
<h3><u>Full Question:</u></h3>
The following compound has been found effective in treating pain and inflammation (J. Med. Chem. 2007, 4222). Which sequence correctly ranks each carbonyl group in order of increasing reactivity toward nucleophilic addition?
A) 1 < 2 < 3
B) 2 < 3 < 1
C) 3 < 1 < 2
D) 1 < 3 < 2
<h3><u>Answer: </u></h3>
The rate of nucleophilic attack of carbonyl compounds is 2<3 <1.
Option B
<h3><u>Explanation. </u></h3>
Nucleophilic attack is explained as the attack of an electron rich radical to a carbonyl compound like aldehyde or a ketone. A nucleophile has a high electron density, so it searches for a electropositive atom where it can donate a portion of its electron density and become stable.
A carbonyl compound is a
hybridized carbon atom with a double bonded oxygen atom in it. The oxygen atom pulls a huge portion of electron density from carbon being very electropositive.
In a ketone, there are two factors that make it less likely to undergo a nucleophilic attack than aldehyde. Firstly, the steric hindrance of two carbon groups being attached with the carbonyl carbon makes it harder for the nucleophile to approach. Secondly, the electron push by the carbon groups attached makes the carbonyl carbon a bit less electropositive than the aldehyde one. So aldehydes are more reactive towards a nucleophilic addition reaction.
Answer:
2.76 (full answer) 2.7617e-6
Explanation: