For cyclohexane compounds drawn in a chair conformation: -axial bonds are vertical -equatorial bonds are parallel to two bonds within the ring. thus, as i assume the chair conformation is drawn: -the x group is in an axial position, as are the five other vertical bonds. -three axial bonds are on the top face of the ring -the other three axial bonds are on the bottom face the position of the second substituent on each ring carbon is equatorial. gauche groups must be on an adjacent carbon such as carbon 6 and carbon 2, and also gauche groups are rotated by 60 degrees relative to each other. drawing the newman projections for c1–c2 and c1–c6 aids in visualizing the groups that are gauche to the y group on c1. click this link and watch some academic videos that may you more understand the topic
Answer from: Quest
girl imma just put my comment here because i need a couple point okurrttt
Look at the spectrums of a star moving towards earth and a motionless star. which of these is a correct inference that can be draw from the observation of the two spectrums? (2 points) the spectrum of a motionless star is difficult to be viewed separately using oridinary telescopes. the spectrum of a motionless star is identical to the spectrum of a star which moves towards earth. the spectrum of a star shifts towards the red region when the star moves towards earth. the spectrum of a star shifts towards the blue region when the star moves towards earth.