Answer:
The compound a is 1-methyl cyclohexene (see attachment for structure).
Explanation:
The reaction of 1-Bromo-1-methylcyclohexane with sodium methoxide is a <u>second-order reaction</u> since the <u>methoxide ion is a strong base</u> and also a strong nucleophile. This ion attacks the alkyl halide faster than the alkyl halide can ionize to produce a first-order reaction. However, we can not see the product of nucleophilic substitution. The SN₂ mechanism is blocked due to the <u>impediment of the 1-Bromo-1-methylcyclohexane</u>. The main product, according to the Zaitsev rule, is the 1-methyl cyclohexene, thus forming a <u>double bond</u>.
Then, this cyclohexene is hydrogenated to form the cyclohexane.
Glycerol will react with 3 butanoic acid molecule to produce glyceryl tributyrate.
Explanation:
You may find the chemical reaction and the structure of molecules in the attached picture.
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triglyceride
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Answer: B) 2 (as indicated by electron distribution shown), but taking into account the real properties of this element, 4,7,8 also occur (see below).
Explanation:
This is the electron complement/atomic number of ruthenium, which actually has the structure [Kr] 5s1 4d7
Nevertheless, Ru does not form Ru(I) compounds and few Ru(II) compounds (RuCl2, RuBr2, RuI2). It also forms Ru(III)Cl3 and a larger number of Ru(IV) compounds, e.g. RuO2, RuS2. It also forms RuO4
The IUPAC name for the given product is 2 chloro Butane.
<h3>What is IUPAC nomenclature?</h3>
IUPAC stands for 'International Union of Pure and Applied Chemistry', which givers some rule for designing the name of compounds of chemistry.
- In the given product total four carbon atoms are present and between all of them single bonds are present.
- In the second carbon atom, chlorine group is present.
- During the nomenclature process, first we write down the name of the attached group which is followed by the alkane chain.
Hence name of the product is 2 chloro Butane.
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Eukaryotic celss have organelles which perform specific functions
