Could anyone help me with questions 2 and 3? I selected answers for both but I\'
ID: 569804 • Letter: C
Question
Could anyone help me with questions 2 and 3? I selected answers for both but I'm not 100% sure they're accurate. Also, could you give an explanation of how you got your answers, thank you
ard ecuedu/webapps assessment/take launch jsp?course assessment id 488971 1&course; d= 4369581 & on YouTube LetMeWatchThis I. Sr MSN.com Watan Wree movies ? ando QUESTION 3 What is the basis for angle strain in cyclobutane? Cyclobutane has no angle strain The staggered arrangement of all the adjacent C-H bonds Poor overlap of sp3 hybrid orbitals between carbons due to bond angles that are much less than 1095o than 1200 QUESTION 4 Which 1.2-disubstituted cyclohexane is a cis isomer? CH3 ChsExplanation / Answer
3)
C-C bond in cyclobutane is partially banana bond. This bond formed when there are weak overlap between sp3 orbitals of two adjacent carbons.
Hence third option is the answer.
2) During hyperconjugation, both sigma and anti bonding sigma MO come in same direction otherwise overlap can not occur.
During this all the other substituents or atoms in adjacent carbons come in eclipsing condision.
so there are high steric strain which leads to decrease the stability of conformation.
Hence third option is the answer.