Answer: yo sorry this a hard one
Explanation:
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Gold has a heavy enough nucleus that its electrons must travel at speeds nearing the speed of light to prevent them from falling into the nucleus. This relativistic effect applies to those orbitals that have appreciable density at the nucleus, such as s and p orbitals. These relativistic electrons gain mass and as a consequence, their orbits contract. As these s and (to some degree) p orbits are contracted, the other electrons in d and f orbitals are better screened from the nucleus and their orbitals actually expand.
Since the 6s orbital with one electron is contracted, this electron is more tightly bound to the nucleus and less available for bonding with other atoms. The 4f and 5d orbitals expand, but can't be involved in bond formation since they are completely filled. This is why gold is relatively unreactive.
Hope it helps
Answer:
☞rock cycle
=> The rock cycle is a basic concept in geology that describes transitions through geologic time among the three main rock types: sedimentary, metamorphic, and igneous. Each rock type is altered when it is forced out of its equilibrium conditions.
=> There are three main kinds of rocks: igneous rock, metamorphic rock, and sedimentary rock. ... It can erode into sediment or melt into magma. It is formed under extreme pressure and temperature deep inside mountain chains.
Explanation:
The correct answer you are looking for is napalm
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Alkenes on reacting with ozone results in the formation of ozonide which undergo reductive cleavage in presence of dimethyl sulfide to form carbonyl compounds (aldehyde or ketone). Whereas in presence of hydrogen peroxide it undergoes oxidative cleavage to form carboxylic acids or ketones.
Since, A alkene yields 4-heptanone only on treatment with ozone and DMS thus, it implies that both the chains on the side of the double-bond are similar the product is 4-heptanone that means the double bond is present between the chains at the 4th carbon. Therefore the structure of compound A is 4,5-dipropyloct-4-ene.
The reaction is as shown in the image.
The reaction of A with m-CPBA (meta-perchlorobenzoic acid) followed by aqueous acid
is shown in the image.
m-CPBA (meta-perchlorobenzoic acid) is a peracid and forms epoxides on reacting with alkenes.