For a molecule to be chiral molecule
It should contain chiral carbon and shouldn't have internal plane of symmetry
Let's first define what is a chiral Carbon
A chiral carbon is a carbon that is attached with four different groups
Now
Internal plane of symmetry :It is a plane that divides the molecule which are mirror images to each other
So
In the first one
A)
There are two chiral carbons
Both the carbons are attached with four different groups
But it has a internal plane of symmetry horizontally
Despite containing chiral carbon it is not a chiral molecule as it has internal plane of symmetry
B)
There are two chiral carbons
Both the carbons are attached with four different groups
It doesn't have an internal plane of symmetry
So it is a chiral molecule
which of these structures represents a chival eta molecule? B) tot 3 - CH₂ EXPLAIN.
B of 25 > Two posssible Lewis structures for the molecule CH, S are given. Determine the formal charge on each atom in both structures. Answer Bank :C - HH HH Which structure is the best Lewis structure for CH,S? The structure with sulfur as the central atom. The structure with carbon as the central atom.
Two posssible Lewis structures for the molecule CH, S are given. Determine the formal charge on each atom in both structures. Answer Bank Which structure is the best Lewis structure for CH S? The structure with carbon as the central atom. The structure with sulfur as the central atom.
3. 14 points: Consider the two molecules below: Molecule A Molecule B CH(CH3)2 CH(CH3)2 1 CH I ICH₃ 27 [ 2 CH3 a. Molecules A and B both have three chiral carbons (labeled 1, 2, and 3). How many unique stereoisomers does 1-isopropyl-2,3-dimethylcyclohexane have? b. Molecules A and B are pairs. C. Determine the configuration (R or S) of chiral carbons 1, 2, and 3 for both molecules. Chiral Carbon Molecule A Molecule B d. Draw the two 'chair' conformers...
narizontal elie Same 22 Which molecule represents the chair-flipped conformer of the given compound? CH CHs CHsCH ring flip Нс" CH,CH CH CH CH снсH CH,CH CH-сн, CHyCH сHнсH нсн,с. CH CH) сH,сH сн, CHCH CHyCH CH IV ш V d. III IV a. e. II b. I c. V
Which is a stronger acid? Must explain with both, words and
structures.
Which is a stronger base? Must explain with both, words and
structures.
. Propose a mechanism for the following reaction:
2. a) Which is a stronger acid? Must explain with both, words and structures.10 pts. LOH OH 8 or b) Which is a stronger base? Must explain with both, words and structures. 5 pts. 3. Propose a mechanism for the following reaction: 15 pts. OH CH, CH H2SO4...
22. Which molecule represents the chair-tripper plecule represents the chair-flipped conformer of the given compound CHOH Н . CHCH CHON снен, CH.CH Hone CHÚC CH.CH CH, CH.CH IV d. IV a. b. II V e.
Which of the following structures represent the same molecule? CH3 1 CH2CH2CH2CH2CH2CH3 4 CH3CH2CH2CH3 CH3 2 CH CH CH CH.CH 5 CH CH.CH,CH,CH; CH CHZ 3 CH3CH2CH2CH2CH2 6 CH CH CH.CH.CH 1.CH.CH; CH, CH,
Question 69 (1 point) Which is the correct IUPAC name for this molecule? CH, CH, CH? CH2 CH; C-CH2-CH2-CH-CH2 CH2 CH2 CH 4,7-diethyl-7-methylnonane 2,2,5,6-tetraethylhexane 1,2,5,5-tetraethylhexane O 3,6-diethyl-3-methylnonane 2,2,5-triethyloctane Question 70 (1 point) What is the geometry and hybridization state of carbon #2 in the compound 1,4- dibromo-1-pentyne? trigonal planar, sp tetrahedral, sp O trigonal planar, sp2 O linear, sp2 linear, sp O linear, sp3 O tetrahedral, sp2 O trigonal planar, sp tetrahedral, sp Question 71 (1 point) Which of these...
Which is not a stable molecule ? If you can explain me how to
understand if it is stable molecule or not , it will be
appreciated
50. The nitrite ion, NO can be represented as a resonance hybrid of two significant Lewis structures. Which statements about this are correct? I. The two resonance structures contribute equally to the Structure. II. The formal charge of nitrogen is zero in both resonance structures. (A) I only (B) II only (C) oth...
4.40 Convert the condensed structures shown to skeletal structures. a. CH3CH2CH=CH2 b. CH CH CH CH OH c. CH3CHCH CH3CH2CHCH2CH2CH3