Answer:
In given structure of substituted cyclohexane select the "Bromine" atom as the answer.
Explanation:
1,3-Diaxial Interactions:
As cleared from name, this type of interactions are found in cyclic alkanes in which one group present at position 1 (assumed number) experiences steric hindrance due to another group present at position 3.
Also, it is necessary that both the groups must be occupying either axial or equatorial positions respectively. For example, in given structure the methyl group at position 1 is at axial position and another bulky group which should interact with this methyl group must occupy axial position at carbon 3 next to carbon 1. Hence, as shown in figure, the Bromine atom is present at third carbon and is at axial position too.
In attached picture, the green lines indicate steric interactions between Methyl group and Bromine atoms which are involved in steric interactions in 1,3-diaxial fashion.
The molar mass of NH4NO3 in g/mol is 80g/mol.
HOW TO CALCULATE MOLAR MASS:
The molar mass of a compound can be calculated by summing the atomic masses of its constituent elements.
In ammonium nitrate (NH4NO3), there are nitrogen, hydrogen, and oxygen elements.
- Atomic mass of nitrogen = 14
- Atomic mass of oxygen = 16
- Atomic mass of hydrogen = 1
Molar mass of NH4NO3 = 14 + 1(4) + 14 + 16(3)
Molar mass of NH4NO3 = 80g/mol
- Therefore, the molar mass of NH4NO3 in g/mol is 80g/mol.
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Answer:
The three-step synthesis of trans-2-pentene from acetylene is as follows.
<u>Step -1:</u> Formation of higher order terminal alkyne on reaction with sodium acetylides with haloalkanes.
<u>Step -2:</u> Formation terminal alkyne to nonterminal alkynes.
<u>Step -3:</u> Formation of trans-pent - 2-pent-ene by reduction.
Explanation:
Synthesis of trans-pent-2-yne from ethyne takes place is mainly a three step synthesis which involves formation of higher order terminal alkyne on reaction with sodium acetylides with haloalkane. Second step involves the further alkylation of terminal alkynes to higher order nonterminal alkynes and the third step involves the formation of trans-2-ene by dissolving reduction method.
The chemical reaction of each step of chemical reactions is as follows.
B:Creates energy through fusion reactions