Let us check each statement one by one
a) Sb has a lower ionization energy but a higher electronegativity than I. : As per values given : Definitely Sb has lower ionization energy however the electronegativity of Sb is lower than that of iodine
b) Sb has a higher ionization energy but a lower electronegativity than I. FAlse:
Sb has lower ionization energy than I
c) Sb has a lower ionization energy and a lower electronegativity than I. True
d) Sb has a higher ionization energy and a higher electronegativity than I. False
Answer:
<u>Frederich Miescher</u>- first person to isolate DNA and RNA
<u>Frederick Griffith</u>- first to demonstrate horizontal transmission of dna using bacteria
<u>Gregor Mendel</u>- documented and demonstrated inheritance patterns
Thomas Hunt Morgan- identified chromosomes as the structures responsible for inheritance
<u>Joachim Hammerling</u>- demonstrated that the hereditary information of of eukaryotes is contained within the nucleus
<u>Alfred Hershey and Martha Chase</u>- demonstrated that dna not protein was the molecule responsible for hereditary
<u>George Beadle and Edward Tatum</u>- used mutants to show the relationship between DNA and proteins
<u>Albrecht Kossel</u>- characterized the structure of adenine, guanine, cytosine, thymine, and uracil
Explanation:
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Answer:
The four resonance structures of the phenoxide ion are shown in the image attached
The conjugate base of cyclohexanol has only one resonance contributor, while
the conjugate base of phenol has four resonance contributors.
Explanation:
In organic chemistry, it is known that structures are more stable if they possess more resonance contributors. The greater the number of contributing canonical structures, the more stable the organic specie. Since the phenoxide ion has four contributing canonical structures, it is quite much more stable than cyclohexanol having only one contributing structure to its conjugate base. Hence the PKa(acid dissociation constant) of phenol is lesser than that of cyclohexanol. The conjugate base of phenol is stabilized by resonance.
Answer:
Draw structures corresponding to the following IUPAC names:(a) (Z)-2-Ethyl-2-buten-1-ol (b) 3-Cyclohexen-1-ol(c) trans-3-Chlorocycloheptanol (d) 1,4-Pentanediol(e) 2,6-Dimethylphenol (f ) o-(2-Hydroxyethyl)phenol
Explanation:
According to IUPAC rules, the name of a compound is:
Prefix+root word+suffix
1) Select the longest carbon chain and it gives the root word.
2) The substituents give the prefix.
3) The functional group gives the secondary suffix and the type of carbon chain gives the primary suffix.
The structure of the given compounds are shown below: