Answer:
They have similar properties, because they share similar amounts of electrons in their outer shell, valence electrons! This means they will only be able to interact with other elements with those electrons so they often show similar properties.
Explanation:
Answer:
See explanation
Explanation:
For a reaction that proceeds by E1 mechanism, the rate determining step involves the formation of the carbocation.
The rate of formation of this carbocation depends only on the concentration of the t-butyl bromide since it is the only specie that enters into the rate equation.
Hence, when the concentration of t-butyl bromide is tripled, the rate of reaction is tripled.
Methanol does not enter into the rate equation hence doubling its concentration does not affect the rate of reaction.
Answer:
Explanation:
Formula
Heat = m * c * delta t
t = temperature in centigrade.
The first thing you have to do is convert kelvin degrees to centigrade. The conversion factor is - 273. The formula is degrees centigrade = degrees kelvin - 273. It is easier to understand with a couple of examples.
- 290o K = 290 - 273 = 17
- 325. K = 325 - 273 = 52
Solution
Heat = 100.0 grams * 4.18 J/g*C * (52 - 17)
Heat = 100 * 4.18 * 35
Heat = 14630 Joules
But you want kj
Heat = 14630 / 100 = 14.63
Answer
Heat = 14.6 kj
Answer:
Hi
Williamson's ether reactions imply that an alkoxide reacts with a primary haloalkane. Alkoxides consisting of the conjugate base of an alcohol and are formed by a group R attached to an oxygen atom. They are often written as RO–, where R is the organic substituent (Step 1).
Sn2 reactions are characterized by the reversal of stereochemistry at the site of the leaving group. Williamson's synthesis is no exception and the reaction is initiated by the subsequent attack of the nucleophile. This requires that the nucleophile and electrophile be in anti-configuration (Step 2).
As an example (figure 3).
In the attached file are each of the steps of Williamson's synthesis.
Explanation:
Explain, in terms
of both atoms and molecular structure, why there is no isomer of CH3OH.
There is no isomer of CH3OH or methanol because it
contains only one carbon atom. And also, the structure is tetrahedral, having
four substances attached to the carbon atom.
